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Clinical Trial Summary

To evaluate the effectiveness of PriMatrix, PriMatrix Ag, and Standard of Care in the treatment of venous leg ulcers (VLUs).


Clinical Trial Description

Healing percentages ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01612806
Study type Interventional
Source Integra LifeSciences Corporation
Contact
Status Terminated
Phase N/A
Start date June 2011
Completion date February 2017

See also
  Status Clinical Trial Phase
Terminated NCT00534937 - Flexitouch Compression System for Venous Stasis Ulcer Phase 4
Terminated NCT01853384 - Safety and Efficacy Trial of HP802-247 in the Treatment of Chronic Venous Leg Ulcers Phase 3
Enrolling by invitation NCT02813187 - Venous Leg Ulcer and Lymphedema Registry
Completed NCT03881267 - SkinTE® in the Treatment of Venous Leg Wounds N/A
Terminated NCT01376050 - Efficacy Study of the Application of Low Level Laser Light to Treat Venous Stasis Ulcers N/A
Completed NCT00900029 - Safety Follow-Up to HP 802-247-09-015 N/A
Completed NCT02626156 - Cooling Leg and Foot Ulcer Skin Post Healing to Prevent Ulcer Recurrence Phase 2
Recruiting NCT02322554 - Cellular and Tissue Based Therapy Registry
Recruiting NCT02467998 - Negative Pressure Wound Therapy Registry
Recruiting NCT04647240 - Dermacyte® Amniotic Wound Care Liquid for the Treatment of Non-Healing Venous Stasis Ulcers Phase 2
Completed NCT02395302 - Evaluation of a Dual Action Pneumatic Compression System: Tolerance and Comfort in Patients With Venous Leg Ulcers N/A
Completed NCT00270946 - Evaluation of Bilayered Cellular Matrix (OrCel) for the Treatment of Venous Ulcers N/A