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A Clinical Study of the Safety and Efficacy of MEBO Wound Ointment in Subjects With Diabetic Foot Ulcers

Diabetic Foot Ulcers Clinical Trial

Official title:
A Phase II, Randomized, Controlled, Multi-Center Study of the Safety and Efficacy of Topically Applied MEBO Wound Ointment Compared to Standard of Care in Subjects With Diabetic Foot Ulcers

Clinical Trial Summary

The objective of this study is to evaluate the safety and efficacy of MEBO in the treatment of subjects with diabetic foot ulcers (DFUs).

Clinical Trial Description

This is a phase II, randomized, controlled, multi-center study designed to assess the safety and efficacy of MEBO in the treatment of subjects with DFUs. Subjects meeting entry criteria will be randomly assigned in a 1:1 ratio for up to 8 weeks of treatment with either MEBO or SOC. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01070433
Study type Interventional
Source Skingenix, Inc.
Contact
Status Completed
Phase Phase 2
Start date September 2012
Completion date December 2013
View Details
See also
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