Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting
43 studies found for:    "cutis laxa"
Show Display Options
RSS Create an RSS feed from your search for:
"cutis laxa"
Need help? See RSS Feeds
Choose a feed type:
Show studies that were first received in the last 14 daysShow studies that were first received in the last 14 days
Show studies added or modified in the last 14 daysShow studies that were added or modified in the last 14 days
Rank Status Study
1 Active, not recruiting Radiofrequency and Pulsed Electromagnetic Field Treatment of Skin Laxity of the Mon Pubis, Labia and Vaginal Introitus
Condition: Skin Laxity
Intervention: Device: Venus Freeze Diamond Polar
2 Terminated Structural Analysis of Human Tissue
Condition: Cutis Laxa
Intervention:
3 Completed Feasibility Study: Higher Density Ulthera® System Treatment With Vectoring for Treatment of the Face and Neck
Condition: Skin Laxity
Intervention: Device: Ulthera System Treatment
4 Completed
Has Results
Lifting and Tightening of the Face in Subjects With Skin of Darker Color
Condition: Facial Skin Laxity
Intervention: Device: Ulthera® System treatment
5 Completed Feasibility Study: Evaluation of the Ulthera® System for Treatment of the Knees
Condition: Skin Laxity
Intervention: Device: Ulthera® System
6 Recruiting Topical Bimatoprost for Chemical Blepharoplasty
Condition: Dermatochalasis
Intervention: Drug: bimatoprost 0.03% ophthalmic solution
7 Completed
Has Results
Application of the Apsara Thermal Wand System
Condition: Tightening of Skin Laxity
Intervention: Device: Apsara Thermal Wand System
8 Completed
Has Results
Ultherapy™ Treatment Following Sculptra® Treatment
Condition: Skin Laxity
Interventions: Device: Ulthera® System;   Drug: Sculptra®;   Other: Sculptra® treatment followed by Ultherapy™ treatment
9 Recruiting Safety and Effectiveness Evaluation of the Device in Achieving Submental Lift
Condition: Skin Laxity
Intervention: Device: Percutaneous Radiofrequency single treatment
10 Active, not recruiting Simulines Non-Inferiority Pivotal Study
Condition: Skin Laxity
Interventions: Device: Ultherapy®;   Device: Standard transducer;   Device: Simulines transducer
11 Completed Retrospective Evaluation of Combination Treatment With the Ulthera System
Condition: Skin Laxity
Interventions: Device: Ultherapy;   Drug: Incobotulinumtoxin A;   Device: Radiesse;   Device: Belotero Balance
12 Recruiting Gene Expression Following Ultherapy® Treatment
Condition: Skin Laxity
Intervention: Device: Ultherapy Treatment
13 Completed Ultherapy® for Treating the Face and Neck Using Standard Versus Simulines Transducers
Condition: Skin Laxity
Interventions: Device: Ulthera Treatment at EL2;   Device: Ulthera Treatment at EL4
14 Withdrawn Combination of Ultrasound Treatment and Neck Liposuction for Skin Tightening
Condition: Skin Laxity
Interventions: Procedure: Neck Liposuction and Ultrasound Treatment;   Procedure: Sham Treatment
15 Completed
Has Results
Treatment of the Face and Neck With Lower Ulthera System Energy Settings
Condition: Skin Laxity
Intervention: Device: Ulthera System Treatment
16 Terminated Feasibility Study: Histological Characterization After Treatment With the Ulthera® System
Condition: Skin Laxity
Intervention: Device: Ulthera Treatment
17 Completed Feasibility Study: Lifting and Tightening Neck Skin in Patients
Condition: Skin Laxity
Intervention: Device: Ulthera System Treatment
18 Completed
Has Results
Feasibility Study: Heavy Water Tissue Labeling Protocol
Condition: Skin Laxity
Interventions: Device: Ulthera® System Treatment;   Other: Heavy Water
19 Completed Feasibility Study: Compare the Effectiveness Between Two Pain Medications When Used Prior to Ultherapy™ Treatments
Condition: Skin Laxity
Interventions: Drug: Advil;   Drug: Lortab;   Device: Ulthera System Treatment
20 Completed Feasibility Study: Ulthera Treatment of the Buttocks and Thighs
Condition: Skin Laxity
Intervention: Device: Ulthera System Treatment

   Previous Page Studies Shown (1-20) Next Page (21-40) Show next page of results    Last Page
Study has passed its completion date and status has not been verified in more than two years.