Trial record 13 of 24 for:    Open Studies | "Complex Regional Pain Syndromes"

Two Measures of Tactile Acuity in CRPS Type I Patients

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2013 by Ruhr University of Bochum
Sponsor:
Information provided by (Responsible Party):
Christoph Maier, Prof. Dr., Ruhr University of Bochum
ClinicalTrials.gov Identifier:
NCT01888783
First received: June 25, 2013
Last updated: August 1, 2013
Last verified: June 2013
  Purpose

This study aims to investigate whether two different measures of tactile acuity lead to comparable results in patients diagnosed with CRPS Type I of the upper extremity. Additionally patients with a neuropathy of the median nerve and healthy controls are included.


Condition Intervention
CRPS Type I of the Upper Extremity
Neuropathy of the Median Nerve
Healthy Controls
Other: Tactile acuity measured by 2PD and the GOT

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Official Title: Comparison of Two Measures of Tactile Acuity in CRPS Type I Patients , Patients With a Neuropathy of the Median Nerve and Healthy Controls.

Resource links provided by NLM:


Further study details as provided by Ruhr University of Bochum:

Primary Outcome Measures:
  • tactile acuity as measured by 2-point-discrimination [ Time Frame: unique measurement of maximal one hour duration ] [ Designated as safety issue: No ]
    Thresholds on the tip of the index finger of boths hands are assessed using the method of constant stimuli. One single needle and seven pairs of needles with different spacings are tested in randomized order. After each presentation, the subject has to report the sensation of one or two needles by answering immediately "one" or "two." Each distance is presented eight times resulting in 64 single decisions. The summed responses are plotted against distance as a psychometric function for absolute threshold and get fitted by a binary logistic regression. Thresholds are taken from the fit at the distance at which 50% correct answers are given

  • tactile acuity as measured by the Grating Orientation Task (GOT) [ Time Frame: unique measurement of maximal half an hour duration ] [ Designated as safety issue: No ]
    Stimuli are taken from a set of dome-shaped plastic gratings with equal groove and ridge widths. Gratings are applied to the immobilized distal fingerpad of the index finger of boths hand with the ridges oriented either along or across the long axis of the finger in randomized sequences of the two alternatives. Subjects have to report the orientation of the gratings as "along" or "across". The largest groove widths in the set is 6mm, the minimal width is 0.5mm. Thresholds were taken from the groove width at which the performance was 75% correct. Unless the performance is exactly 75% for a particular grating, interpolation between gratings spanning the 75% correct responses ared used


Other Outcome Measures:
  • Touch threshold for light touch [ Time Frame: unique measurement, duration approx. 5 minutes ] [ Designated as safety issue: No ]
    Touch thresholds are taken from a set of von Frey filaments (0.25 mN - 512 mN). Touch sensitivity is investigated by using a staircase procedure during which subjects are required to close their eyes and report when they perceive an indentation of the skin on the fingerpad of the index finger. The applied forces are decreased in a stepwise manner until the subject no longer perceives the stimulus (lower boundary) and then increased until the stimulus is perceived again (upper boundary). This procedure is repeated 5 times resulting in 10 values that are averaged to provide the touch threshold.


Estimated Enrollment: 150
Study Start Date: September 2012
Estimated Study Completion Date: September 2013
Estimated Primary Completion Date: September 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: CRPS Type I
Patients diagnosed with complex regional pain syndrome type I of the upper limb
Other: Tactile acuity measured by 2PD and the GOT
For a detailed description of the methods see "outcome measures"
Other Names:
  • 2-point-discrimination (2PD)
  • Grating Orientation Task (GOT)
Active Comparator: Median Nerve Neuropathy
Patients diagnosed with a neuropathy of the median nerve of the upper limb.
Other: Tactile acuity measured by 2PD and the GOT
For a detailed description of the methods see "outcome measures"
Other Names:
  • 2-point-discrimination (2PD)
  • Grating Orientation Task (GOT)
Active Comparator: Healthy Controls
Healthy adult persons.
Other: Tactile acuity measured by 2PD and the GOT
For a detailed description of the methods see "outcome measures"
Other Names:
  • 2-point-discrimination (2PD)
  • Grating Orientation Task (GOT)

  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Patients diagnosed with CRPS Type I according to the "Budapest Criteria"
  • Patients diagnosed with a neuropathy of the median nerve
  • Healthy Controls,matched in age and gender to both patient cohorts

Exclusion Criteria:

  • intolerable hyperalgesia
  • lesions at the fingertips
  • high grade digit contracture
  • central neurologic disorders
  • psychiatric disorders
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01888783

Contacts
Contact: Christoph Maier, Prof. Dr. +49 2343023402 Christoph.Maier@rub.de
Contact: Marianne David, Dr. +49 2343023324 Marianne.David@rub.de

Locations
Germany
Department of Pain Medicine, BG Universitätsklinikum Bergmannsheil GmbH Recruiting
Bochum, Germany, 44789
Contact: Christoph Maier, Prof. Dr.    +49 2343023402    Christoph.Maier@rub.de   
Contact: Marianne David, Dr.    +49 2343023324    Marianne.David@rub.de   
Principal Investigator: Christoph Maier, Prof.Dr.         
Sponsors and Collaborators
Ruhr University of Bochum
Investigators
Study Chair: Christoph Maier, Prof. Dr. Ruhr University Bochum
  More Information

No publications provided

Responsible Party: Christoph Maier, Prof. Dr., Prof. Dr. med Christoph Maier, Head Dep. of Pain Medicine, Ruhr University of Bochum
ClinicalTrials.gov Identifier: NCT01888783     History of Changes
Other Study ID Numbers: GOT_CRPS2013
Study First Received: June 25, 2013
Last Updated: August 1, 2013
Health Authority: Germany: Ethics Commission

Keywords provided by Ruhr University of Bochum:
CRPS Type I
tactile acuity
2-point-discrimination
Grating Orientation Task
sensory signs

Additional relevant MeSH terms:
Complex Regional Pain Syndromes
Autonomic Nervous System Diseases
Nervous System Diseases
Peripheral Nervous System Diseases
Neuromuscular Diseases

ClinicalTrials.gov processed this record on August 27, 2014