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Clinical Trial Summary

In this study, the investigators hypothesize that the use of olivamine-containing products in the management of patients with compromised nonhealing lower extremity ulcers is feasible in the Philippine setting. It will result in complete ulcer healing or wound closure after 16 weeks.


Clinical Trial Description

The specific aim of this study is to assess the feasibility of using olivamine-containing products in the management of patients with compromised nonhealing lower extremity ulcers in the Philippines. The primary endpoint of which is to evaluate the efficacy of Olivamine on healing of chronic lower extremity ulcers which will be assessed by rate of change in ulcer size (wound healing trajectory) and proportion with complete ulcer healing (wound closure) at 4, 8, 16 and 16 weeks compared to baseline, week 0. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01657318
Study type Observational
Source De La Salle University Medical Center
Contact
Status Terminated
Phase
Start date September 1, 2012
Completion date February 15, 2013

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