| 1 |
NCT03260400 |
Recruiting |
Short-term Implanted Electrodes Following Regenerative Peripheral Nerve Surgery for Improving Prosthetic Limb Control Signals |
- Amputation Neuroma
- Amputation
|
- Device: a bipolar percutaneous intramuscular electromyography electrode
|
Interventional
|
Not Applicable |
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Basic Science
|
- Change in Pain Level as measured by SF-36
- Change in Pain Level as measured by LANSS surveys
- RPNI tissue degeneration measured by volume during ultrasound
- (and 3 more...)
|
10 |
All |
22 Years and older (Adult, Older Adult) |
NCT03260400 |
HUM00124839 |
|
July 19, 2017 |
July 2023 |
July 2023 |
August 24, 2017 |
August 24, 2017 |
|
- University of Michigan
Ann Arbor, Michigan, United States
|
|
| 2 |
NCT03433300 |
Recruiting |
Microprocessor Knees in Early Rehabilitation |
|
- Device: Ottobock Kenevo
- Device: Ottobock 3R60/3R62
|
Interventional
|
Not Applicable |
- University of Washington
- United States Department of Defense
- Otto Bock Healthcare Products GmbH
|
Other / U.S. Fed / Industry |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Outcomes Assessor)
- Primary Purpose: Treatment
|
- Prosthetic Limb Users Survey of Mobility
- Fall frequency
- Daily step count
- (and 7 more...)
|
24 |
All |
18 Years and older (Adult, Older Adult) |
NCT03433300 |
STUDY00003524 |
|
April 13, 2018 |
September 2020 |
September 2020 |
February 14, 2018 |
April 17, 2018 |
|
- University of Washington
Seattle, Washington, United States
|
|
| 3 |
NCT03505983 |
Recruiting |
Criteria for Advanced Prosthetic Foot Prescription |
- Prosthesis User
- Amputation; Traumatic, Limb, Lower
|
- Device: ESR Prosthetic Foot First
- Device: Articulating ESR Prosthetic Foot First
- Device: Powered Prosthetic Foot First
|
Interventional
|
Not Applicable |
- VA New York Harbor Healthcare System
- Walter Reed National Military Medical Center
- James A. Haley Veterans Administration Hospital
- VA Puget Sound Health Care System
|
U.S. Fed |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: None (Open Label)
- Primary Purpose: Supportive Care
|
- Change in 6-min walk distance for each prosthetic foot type
- Change in TUG times for each prosthetic foot type
- Change in 4SST times for each prosthetic foot type
- (and 9 more...)
|
120 |
All |
18 Years and older (Adult, Older Adult) |
NCT03505983 |
IRB #01603
Award Number W81XWH-17-2-0014 |
|
August 1, 2017 |
September 30, 2020 |
September 30, 2021 |
April 23, 2018 |
April 27, 2018 |
|
- VA New York Harbor Healthcare System
New York, New York, United States
|
|
| 4 |
NCT00985881 |
Recruiting |
Use of Subtle Vibration to Improve Walking Ability by Lower Limb Amputees |
- Amputation
- Diabetes Complications
|
- Device: Custom prosthetic socket with mechanical vibrators (stochastic resonance)
- Device: Conventional prosthetic socket (current clinical practice)
|
Interventional
|
Not Applicable |
- VA Office of Research and Development
- University of Texas
|
U.S. Fed / Other |
- Allocation: Randomized
- Intervention Model: Factorial Assignment
- Masking: Single (Participant)
- Primary Purpose: Treatment
|
|
40 |
All |
18 Years to 70 Years (Adult, Older Adult) |
NCT00985881 |
A4376-R |
|
April 1, 2007 |
February 28, 2020 |
August 30, 2020 |
September 29, 2009 |
May 31, 2018 |
|
- VA Puget Sound Health Care System Seattle Division, Seattle, WA
Seattle, Washington, United States
|
|
| 5 |
NCT03027947 |
Recruiting |
Spinal Root and Spinal Cord Stimulation for Restoration of Function in Lower-Limb Amputees |
- Traumatic Amputation of Lower Extremity
- Phantom Limb Pain
|
- Device: Spinal cord stimulator
|
Interventional
|
Not Applicable |
- University of Pittsburgh
- National Institute of Neurological Disorders and Stroke (NINDS)
|
Other / NIH |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Stimulation perceptual thresholds to a variety of stimulus parameters
- Stimulation neurophysiology thresholds to a variety of stimulus parameters
- Location of evoked sensory percepts
- (and 3 more...)
|
10 |
All |
18 Years to 70 Years (Adult, Older Adult) |
NCT03027947 |
PRO16060190
UH3NS100541 |
|
March 16, 2017 |
July 2021 |
July 2022 |
January 23, 2017 |
February 14, 2018 |
|
- University of Pittsburgh
Pittsburgh, Pennsylvania, United States
|
|
| 6 |
NCT02891707 |
Recruiting |
Mobile Device Outcomes-based Rehabilitation Program |
|
- Device: Rehabilitative Lower-limb Orthopedic Accommodating-feedback Device (ReLOAD)
|
Interventional
|
Phase 1
Phase 2 |
- Henry M. Jackson Foundation for the Advancement of Military Medicine
- Walter Reed National Military Medical Center
- Center for Rehabilitation Sciences Research
- (and 2 more...)
|
Other / U.S. Fed |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Supportive Care
|
- Change in Timed Up and Go (TUG)
- Change in Six-minute Walk Test (6MWT)
- Change in Amputee Mobility Predictor (AMP)
- (and 20 more...)
|
150 |
All |
20 Years to 80 Years (Adult, Older Adult) |
NCT02891707 |
407406 |
MDORP |
May 2016 |
May 2019 |
May 2020 |
September 7, 2016 |
August 21, 2017 |
|
- Walter Reed National Military Medical Center
Bethesda, Maryland, United States
|
|
| 7 |
NCT02684201 |
Recruiting |
Epidural Spinal Cord Stimulation for Sensory Restoration and Phantom Limb Pain in Upper-Limb Amputees |
|
- Device: Boston Scientific Stimulator Lead
|
Interventional
|
Not Applicable |
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Stimulation thresholds to a variety of stimulus parameters
- Location and modality of evoked sensory percepts
- Qualitative self-report of evoked sensations
- (and 2 more...)
|
10 |
All |
18 Years to 70 Years (Adult, Older Adult) |
NCT02684201 |
PRO15010131 |
PhantomLimb |
November 2015 |
October 2018 |
December 2019 |
February 17, 2016 |
February 19, 2018 |
|
- University of Pittsburgh
Pittsburgh, Pennsylvania, United States
|
|
| 8 |
NCT02765035 |
Recruiting |
C-Leg 3 and C-Leg 4 Study in Transfemoral Amputees |
- Lower Limb Amputation Above Knee (Injury)
|
- Device: C-Leg 4
- Device: C-Leg 3
|
Interventional
|
Phase 4 |
- Otto Bock Healthcare Products GmbH
|
Industry |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: Double (Participant, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Change in 6 Minute Gait Test
- Change in 10 meter Gait Test
- Change in Stairs Assessment Index (SAI)
- (and 7 more...)
|
20 |
All |
18 Years and older (Adult, Older Adult) |
NCT02765035 |
PD-PS00120010A-001 |
|
April 2016 |
December 2017 |
December 2017 |
May 6, 2016 |
December 14, 2016 |
|
- Orthopedic Rehabilitation Center SKA Zicksee
St. Andrä, Burgenland, Austria - University Leuven
Pellenberg, Belgium
|
|
| 9 |
NCT03517774 |
Not yet recruiting |
Improving Prosthetic Care for Patients With a Lower Limb Amputation |
|
- Device: 3D Printed Socket
|
Interventional
|
Not Applicable |
- Sunnybrook Health Sciences Centre
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Other
|
- Time to Complete Prosthetic Process - SCIL Form
- Costs Associated with Prosthetic Process - SCIL Form
- Satisfaction with Socket Ratings
- Comfort With Socket Ratings
|
20 |
All |
18 Years and older (Adult, Older Adult) |
NCT03517774 |
MaRS 3D-Printing |
|
May 2018 |
June 2018 |
September 2018 |
May 7, 2018 |
May 7, 2018 |
|
|
|
| 10 |
NCT03199222 |
Recruiting |
Prosthetic Smart Socket Technology to Improve Patient Interaction, Usability, Comfort, Fit, and Function. |
- Complications of the Amputated Limb
|
- Device: Prosthetic smart socket technology with patient prompting
|
Interventional
|
Not Applicable |
- University of South Florida
- U.S. Army Medical Research Acquisition Activity
|
Other / U.S. Fed |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Single (Outcomes Assessor)
- Primary Purpose: Other
|
- Intermediate stage prosthetic complications
- Limb volume activity of the residual limb
- Intermediate stage prosthetic complications (clinical documentation)
- (and 3 more...)
|
60 |
All |
18 Years to 60 Years (Adult) |
NCT03199222 |
Pro00026455 |
|
March 29, 2018 |
May 2018 |
July 2019 |
June 26, 2017 |
April 6, 2018 |
|
- University of South Florida
Tampa, Florida, United States
|
|
| 11 |
NCT02666859 |
Recruiting |
Virtual Reality Prosthetic Training and Rehabilitation |
|
|
Interventional
|
Early Phase 1 |
- University of South Florida
- U.S. Army Medical Research and Materiel Command
- Telemedicine & Advanced Technology Research Center
|
Other / U.S. Fed |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Joint Angle Range of Motion
- Movement Symmetry
|
30 |
All |
18 Years to 65 Years (Adult, Older Adult) |
NCT02666859 |
Pro00016934 |
|
January 2016 |
March 2017 |
December 2017 |
January 28, 2016 |
September 27, 2016 |
|
- University of South Florida
Tampa, Florida, United States
|
|
| 12 |
NCT03550118 |
Recruiting
New |
Auto Control of Volume Management for Limb Loss |
- Lower Limb Amputation Below Knee (Injury)
|
- Device: Adjustable socket
|
Interventional
|
Not Applicable |
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Supportive Care
|
- Change in Limb Volume
- Change in Limb Movement
|
50 |
All |
18 Years and older (Adult, Older Adult) |
NCT03550118 |
STUDY00001779 |
|
August 7, 2015 |
October 2019 |
January 2021 |
June 8, 2018 |
June 8, 2018 |
|
- University of Washington Bioengineering
Seattle, Washington, United States
|
|
| 13 |
NCT02540681 |
Recruiting |
Prosthetic Fit Assessment in Transtibial Amputees Secondary to Trauma |
- Traumatic Amputation of Lower Extremity
|
|
Observational
|
|
- Major Extremity Trauma Research Consortium
- University of California, San Francisco
- Major Extremity Trauma Research Consortium
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
- Prosthetic Fit and Alignment
- Reliability of ProFit assessment tool
- Validity of ProFit Assessment tool
- Responsiveness of ProFit Assessment tool
|
60 |
All |
18 Years to 60 Years (Adult) |
NCT02540681 |
OR130357 |
ProFit |
January 2015 |
January 2021 |
July 2022 |
September 4, 2015 |
April 26, 2017 |
|
- University of California at San Francisco
San Francisco, California, United States - Tampa General Hospital
Tampa, Florida, United States - University of Maryland, R Adams Cowley Shock Trauma Center
Baltimore, Maryland, United States - (and 8 more...)
|
|
| 14 |
NCT03532100 |
Recruiting
New |
Pivot-Flex Foot: Optimal Coupling Ratio Between Transverse and Sagittal-plane Motions Using a Torsionally Adaptive Prosthesis for Individuals With Lower Limb Amputation |
- Lower Extremity Amputation
|
- Device: Torsionally adaptive prosthesis with 0:1 coupling ratio
- Device: Torsionally adaptive prosthesis with 1:6 coupling ratio
- Device: Torsionally adaptive prosthesis with 1:4 coupling ratio
- (and 2 more...)
|
Interventional
|
Not Applicable |
- VA Office of Research and Development
|
U.S. Fed |
- Allocation: Randomized
- Intervention Model: Factorial Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Peak transverse-plane prosthetic socket torque
- Satisfaction with the prosthesis
|
15 |
All |
18 Years to 70 Years (Adult, Older Adult) |
NCT03532100 |
A2456-R
RX002456 Part 1
I01RX002456-01A1 |
|
April 18, 2018 |
September 30, 2020 |
September 30, 2021 |
May 22, 2018 |
May 28, 2018 |
|
- VA Puget Sound Health Care System Seattle Division, Seattle, WA
Seattle, Washington, United States
|
|
| 15 |
NCT03204513 |
Recruiting |
Impact of Powered Knee-Ankle Prosthesis Leg on Everyday Community Mobility and Social Interaction |
|
- Device: Vanderbilt Powered Knee-Ankle Prosthesis
- Device: Microprocessor (MP) Knee Prosthesis
|
Interventional
|
Not Applicable |
|
Other |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: None (Open Label)
- Primary Purpose: Device Feasibility
|
- Change between devices of the Modified Graded Treadmill Test
- Change in Biomechanical Assessment [Gait Parameters and Surface Electromyography (EMG) Activation] Between Devices
- Change in Manual Muscle Test (MMT)
- (and 13 more...)
|
15 |
All |
18 Years to 80 Years (Adult, Older Adult) |
NCT03204513 |
STU00200842 |
|
December 2016 |
April 2018 |
April 2020 |
July 2, 2017 |
July 2, 2017 |
|
- Shirley Ryan AbilityLab
Chicago, Illinois, United States
|
|
| 16 |
NCT02835378 |
Recruiting |
Bilateral Upper Limb Amputation Observatory |
- Bilateral Upper Limb Amputation
- Transverse Short Amputation of the Hand
- Arm Amputation
|
|
Observational
|
|
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
- Etiology of amputation
- Amputation level on each side
- Number and indication of surgical interventions
- (and 6 more...)
|
40 |
All |
Child, Adult, Older Adult |
NCT02835378 |
69HCL16_0465 |
ARMOBS |
December 2015 |
December 2020 |
December 2020 |
July 18, 2016 |
July 18, 2016 |
|
- Hospices Civils de Lyon, Hôpital Edouard Herriot
Lyon, France
|
|
| 17 |
NCT02678247 |
Recruiting |
Functional Performance Evaluation of NU-FlexSIV Socket |
- Amputation
- Artificial Limbs
|
- Device: Northwestern University Flexible Sub-Ischial Vacuum Socket
- Device: Ischial Containment Socket
|
Interventional
|
Not Applicable |
- Northwestern University
- United States Department of Defense
- Jesse Brown VA Medical Center
- Scheck and Siress Prosthetics Orthotics
|
Other / U.S. Fed |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: Single (Outcomes Assessor)
- Primary Purpose: Treatment
|
- Difference in Socket Comfort Score (SCS) between IC socket and NU-FlexSIV socket.
- Difference in walking speed between the IC socket and NU-FlexSIV socket.
- Difference in step length between the IC socket and NU-FlexSIV socket.
- (and 9 more...)
|
30 |
All |
21 Years and older (Adult, Older Adult) |
NCT02678247 |
W81XWH-15-1-0708 |
|
April 2016 |
September 2019 |
September 2019 |
February 9, 2016 |
March 29, 2018 |
|
- Jesse Brown VA Medical Center Motion Analysis Research Laboratory
Chicago, Illinois, United States - Northwestern University Prosthetics-Orthotics Center
Chicago, Illinois, United States - Scheck and Siress Prosthetics Orthotics
Oakbrook Terrace, Illinois, United States
|
|
| 18 |
NCT02797457 |
Not yet recruiting |
Medical Economic Evaluation of Bilateral Allograft of Hands and Forearms |
- Bilateral Traumatic Amputation of Upper Limbs
|
- Procedure: Bilateral allograft of the hands and forearms.
- Procedure: Prosthetic forehands
|
Interventional
|
Not Applicable |
|
Other |
- Allocation: Non-Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
|
40 |
All |
18 Years to 60 Years (Adult) |
NCT02797457 |
69HCL15_0084 |
ARMEDIC |
September 2018 |
September 2026 |
September 2026 |
June 13, 2016 |
May 28, 2018 |
|
|
|
| 19 |
NCT02124876 |
Recruiting |
Accommodating for Residual Limb Fluid Volume Change |
- Diurnal Residual Limb Fluid Volume Fluctuation
|
|
Observational
|
|
- University of Washington
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
|
Other / NIH |
- Observational Model: Cohort
- Time Perspective: Prospective
|
- Residual limb fluid volume
- Duration of walking and moving
|
50 |
All |
18 Years and older (Adult, Older Adult) |
NCT02124876 |
STUDY00002557
R01HD060585 |
AM-PM |
June 2013 |
June 2018 |
December 2018 |
April 28, 2014 |
August 24, 2017 |
|
- University of Washington
Seattle, Washington, United States
|
|
| 20 |
NCT03164356 |
Recruiting |
Bioimpedance as a Diagnostic Tool for Assessing the Need for Socket Modification in Transtibial Amputees |
|
- Other: Socket Modification Regime
|
Interventional
|
Not Applicable |
|
Other |
- Allocation: Randomized
- Intervention Model: Sequential Assignment
- Masking: Single (Participant)
- Primary Purpose: Diagnostic
|
- Socket comfort score, measured by how comfortable the patient's limb is within the socket
- Prosthesis satisfaction, measured by the patient's overall satisfaction with their entire prosthesis
- Overall walking, measured by patients' ability to walk while wearing their prosthesis
- (and 36 more...)
|
118 |
All |
18 Years and older (Adult, Older Adult) |
NCT03164356 |
STUDY00000969 |
|
November 9, 2016 |
January 1, 2020 |
January 1, 2020 |
May 23, 2017 |
May 14, 2018 |
|
- University of Washington Bioengineering
Seattle, Washington, United States
|
|
| 21 |
NCT03432325 |
Recruiting |
Neural Enabled Prosthesis for Upper Limb Amputees |
- Amputation Arm and Hand, Unilateral Right
- Amputation Arm and Hand, Unilateral Left
- Prosthesis User
|
- Device: Neural Enabled Prosthesis
|
Interventional
|
Not Applicable |
- Ranu Jung PhD
- Florida International University
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Device Feasibility
|
- Safety of the Neural Stimulation System
- Efficacy: Functionality of implanted system components
- Efficacy: Elicited sensations
- (and 8 more...)
|
6 |
All |
18 Years and older (Adult, Older Adult) |
NCT03432325 |
NEP601 |
|
December 14, 2017 |
January 2020 |
January 2020 |
February 14, 2018 |
March 8, 2018 |
|
- Florida International University
Miami, Florida, United States
|
|
| 22 |
NCT02589080 |
Recruiting |
Phantom Limb Pain: Efficacy of Non-invasive Sensory Feedback Through the Prosthesis |
|
- Behavioral: Non-invasive sensory feedback
|
Interventional
|
Not Applicable |
- Lund University Hospital
- Aalborg Universitetshospital
- University of Freiburg
- (and 6 more...)
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Change in phantom Limb pain
- Cortical reorganization
|
10 |
All |
18 Years to 75 Years (Adult, Older Adult) |
NCT02589080 |
EPIONE-LU |
EPIONE |
January 2015 |
October 2017 |
October 2017 |
October 28, 2015 |
September 8, 2016 |
|
- Fredrik Sebelius
Lund, Sweden
|
|
| 23 |
NCT01964261 |
Recruiting |
Providing Closed Loop Cortical Control of Extracorporeal Devices to Patients With Quadriplegia |
|
- Device: Neural Prosthetic System 2 (NPS2)
|
Interventional
|
Not Applicable |
- Richard A. Andersen, PhD
- University of Southern California
- Rancho Los Amigos National Rehabilitation Center
- California Institute of Technology
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Basic Science
|
- Patient control over the end effector (virtual or physical)
- Absence of infection or irritation
|
2 |
All |
22 Years to 65 Years (Adult, Older Adult) |
NCT01964261 |
HS-13-00492 |
|
November 2013 |
November 2018 |
January 2019 |
October 17, 2013 |
April 18, 2017 |
|
- Rancho Los Amigos National Rehabilitation Center
Downey, California, United States - University of Southern California
Los Angeles, California, United States - California Institute of Technology
Pasadena, California, United States
|
|
| 24 |
NCT02493842 |
Recruiting |
Direct Nerve Stimulation for Treatment of Phantom Limb Pain |
|
- Device: Transverse Intrafasicular Multichannel electrode (TIME)
|
Interventional
|
Not Applicable |
- Aalborg Universitetshospital
- Aalborg University
- University of Lausanne Hospitals
- (and 9 more...)
|
Other / Industry |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Phantom limb pain
- Cortical reorganization
|
4 |
All |
18 Years to 70 Years (Adult, Older Adult) |
NCT02493842 |
EPIONE-602547-5
no. 602547 |
EPIONE |
June 2015 |
September 2017 |
September 2017 |
July 10, 2015 |
August 9, 2016 |
|
- Aalborg University Hospital
Aalborg, Nordjylland, Denmark
|
|
| 25 |
NCT03236012 |
Not yet recruiting |
Hyperhidrosis in Patients With Amputations |
|
- Diagnostic Test: Minor Iodine-Starch Test
- Other: Aluminum Chloride
- Drug: Botulinum toxin type A
|
Interventional
|
Phase 1 |
- Colby Hansen
- Department of Veterans Affairs Medical Center Health Care System
- University of Utah
|
Other |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- Change in Hyperhidrosis Disease Severity Scale.
|
75 |
All |
18 Years and older (Adult, Older Adult) |
NCT03236012 |
OP150030 |
|
October 15, 2017 |
October 15, 2020 |
October 15, 2021 |
August 1, 2017 |
August 1, 2017 |
|
- University of Utah Hospital
Salt Lake City, Utah, United States - George E. Wahlen Department of Veterans Affairs Medical Center
Salt Lake City, Utah, United States
|
|
| 26 |
NCT03390751 |
Recruiting |
Atropine Weight and Risk of Postoperative Confusion in the Elderly |
|
|
Observational
|
|
- University Hospital, Toulouse
|
Other |
- Observational Model: Cohort
- Time Perspective: Prospective
|
- Association between atropine load of medications on the risk of postoperative confusion
- Atropinic load of drugs
- Duration of hospitalization
- (and 2 more...)
|
130 |
All |
65 Years and older (Older Adult) |
NCT03390751 |
RC31/17/0202
2017-A01847-46 |
ATROPAGE |
December 14, 2017 |
January 2020 |
January 2021 |
January 4, 2018 |
January 8, 2018 |
|
- Pierre-Paul-Riquet University Hospital
Toulouse, France
|
|
| 27 |
NCT03416348 |
Not yet recruiting |
Hyperhidrosis, Developing a Treatment Approach Aims 1 & 2 |
|
- Drug: Aluminum Chloride 20% (deodorant)
- Drug: Alcohol
|
Interventional
|
Phase 1 |
- Colby Hansen
- Department of Veterans Affairs Medical Center Health Care System
- University of Utah
|
Other |
- Allocation: Randomized
- Intervention Model: Crossover Assignment
- Masking: Double (Participant, Investigator)
- Primary Purpose: Treatment
|
- Hyperhidrosis Disease Severity Scale (HDSS)
|
50 |
All |
18 Years and older (Adult, Older Adult) |
NCT03416348 |
OP150030 (Aim 1&2)
OP150030 |
|
June 15, 2018 |
October 15, 2020 |
October 15, 2021 |
January 31, 2018 |
May 4, 2018 |
|
- George E. Wahlen Department of Veterans Affairs Medical Center
Salt Lake City, Utah, United States - University of Utah
Salt Lake City, Utah, United States
|
|
| 28 |
NCT03412656 |
Recruiting |
Assessing Force Feedback With the SoftHand Pro |
- Amputation, Traumatic
- Limb Defect
|
|
Interventional
|
Not Applicable |
- Kristin Zhao, PhD
- Arizona State University
- University of Pisa
- Mayo Clinic
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Device Feasibility
|
- Conveyance of force feedback
- Improvement to device embodiment through addition of grip force feedback
|
15 |
All |
18 Years and older (Adult, Older Adult) |
NCT03412656 |
17-005611 |
CUFF |
October 17, 2017 |
December 31, 2018 |
December 31, 2019 |
January 26, 2018 |
March 22, 2018 |
|
- Mayo Clinic in Rochester
Rochester, Minnesota, United States
|
|
| 29 |
NCT03030079 |
Recruiting |
Electrical Stimulus Therapy for Chronic Phantom Limb Pain |
|
- Device: High intensity electrical stimulation
|
Interventional
|
Early Phase 1 |
- University of Colorado, Denver
- Hanger Clinic: Prosthetics & Orthotics
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Use of electrical stimulus medium frequency alternating current for short term decreased Phantom Limb Pan
- Assess the effectiveness of reducing chronic phantom limb pain long term.
|
10 |
All |
18 Years to 85 Years (Adult, Older Adult) |
NCT03030079 |
16-1063 |
|
January 2017 |
December 2018 |
December 2018 |
January 24, 2017 |
May 10, 2018 |
|
- Children's Hospital Colorado Research Institute
Aurora, Colorado, United States
|
|
| 30 |
NCT03389334 |
Recruiting |
Massage on Pain Levels, Range of Motion, and Muscle Strength in Unilateral Lower Limb Amputees |
|
|
Interventional
|
Not Applicable |
|
Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Other
|
- Low Back Pain
- visual analog pain scale
- Range of Motion
- Muscle strength
|
10 |
All |
18 Years and older (Adult, Older Adult) |
NCT03389334 |
5170458 |
|
March 29, 2018 |
December 2018 |
December 2018 |
January 3, 2018 |
April 5, 2018 |
|
- Loma Linda Universtiy
Loma Linda, California, United States
|
|
| 31 |
NCT02682186 |
Recruiting |
Pectoral Nerve Block for Analgesia After Breast Augmentation |
- Ambulatory Plastic Surgery
- Esthetic Prosthetic Breast Expansion
|
- Drug: Ropivacaine after dilution with sodium chloride 0.9%
|
Interventional
|
Phase 3 |
- University Hospital, Montpellier
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: Triple (Participant, Care Provider, Outcomes Assessor)
- Primary Purpose: Treatment
|
- Maximal value of pain intensity according to the numerical scale within the six first hours
- Maximal value of the pain at day 1 and until day 5
- Morphinics side effects such as nausea / vomiting, constipation, pruritus; analgesic consumption, surgical complication, satisfaction questionaire
|
92 |
Female |
18 Years to 70 Years (Adult, Older Adult) |
NCT02682186 |
95832
2015-002368-17 |
PECS B&BS |
February 1, 2016 |
February 1, 2019 |
February 6, 2019 |
February 15, 2016 |
November 6, 2017 |
|
- UH Montpellier - Hôpital Gui de Chauliac
Montpellier, France - UH Montpellier
Montpellier, France - CHU Nîmes
Nîmes, France
|
|
| 32 |
NCT01821976 |
Recruiting |
Transtibial Amputation Outcomes Study |
|
- Procedure: Ertl Procedure
- Procedure: Burgess Procedure
|
Interventional
|
Not Applicable |
- Major Extremity Trauma Research Consortium
- Major Extremity Trauma Research Consortium
|
Other |
- Allocation: Randomized
- Intervention Model: Parallel Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Patient Reported Function
- Number of Revision Surgeries
- Physical Impairment
- (and 2 more...)
|
250 |
All |
18 Years to 60 Years (Adult) |
NCT01821976 |
W8XWH-10-2-0090 |
TAOS |
March 2013 |
January 2021 |
June 2022 |
April 1, 2013 |
June 14, 2017 |
|
- Naval Medical Center San Diego
San Diego, California, United States - University of California San Francisco Medical Center
San Francisco, California, United States - University of Miami Ryder Trauma Center
Miami, Florida, United States - (and 25 more...)
|
|
| 33 |
NCT03178890 |
Recruiting |
Osseointegrated Human-Machine Gateway |
- Amputation
- Osseointegration
- Neuroprostheses
|
|
Interventional
|
Not Applicable |
- Integrum
- Sahlgrenska University Hospital, Sweden
- Chalmers University of Technology
|
Industry / Other |
- Intervention Model: Single Group Assignment
- Masking: None (Open Label)
- Primary Purpose: Treatment
|
- Percentage of total study population with Adverse Events graded as Serious Adverse Events (SAE)
- Number of subjects with at least two independent myoelectric signals, and at least one sensory feedback location
- Significant Improvement (p>0,05) in Myoelectric Control Using the "Assessment of Capacity for Myoelectric Control" (ACMC) Functionality Test
|
18 |
All |
18 Years to 69 Years (Adult, Older Adult) |
NCT03178890 |
007618 |
OHMG |
September 26, 2016 |
February 1, 2020 |
February 1, 2020 |
June 7, 2017 |
June 7, 2017 |
|
- Centre for Advanced Reconstruction of Extremities (CARE), Sahlgrenska University Hospital
Molndal, Sweden
|
|
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