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A Prospective, Randomized, Double-Blind Controlled Study of WPP-201 for the Safety and Efficacy of Treatment of Venous Leg Ulcers — WPP-201  

Venous Leg Ulcers Clinical Trial

Official title:
A Prospective, Randomized Double-Blind Controlled Study of WPP-201 for the Safety and Efficacy of Treatment of Venous Leg Ulcers

Clinical Trial Summary

To test safety and efficacy of Bacteriophage on Venous Leg Ulcers.

Clinical Trial Description

This is a prospective, randomized, controlled double blind study in patients with full thickness venous leg ulcers of greater than 30 days duration evaluating the safety of WPP-201 on the healing of those wounds. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00663091
Study type Interventional
Source Southwest Regional Wound Care Center
Contact
Status Completed
Phase Phase 1
Start date September 2006
Completion date May 2008
View Details
See also
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