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Evaluation of the Initial Safety and Efficacy of Keloid Lesions Treated With MF-4181

Keloid Clinical Trial

Official title:
A Prospective, Randomized, Comparative Feasibility Study Evaluating the Initial Safety and Efficacy of Keloid Lesions Treated With MF-4181 Adjunctive to Surgical Scar Revision

Clinical Trial Summary

The objective of the study is to evaluate the initial safety and efficacy of MF-4181, a hydrogel scaffold, in the reduction of the volume, appearance, and/or symptoms associated with keloid scarring in subjects undergoing surgical revision of keloid scars.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01446770
Study type Interventional
Source Halscion, Inc.
Contact
Status Completed
Phase Phase 2
Start date November 2010
Completion date December 2011
View Details
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