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Celotres for Improvement in Wound Healing and Resulting Scar Consequences Following Suturing of a Wound — PMCS EURO HEAL  

Scar Clinical Trial

Official title:
A Post Market Clinical Study Evaluating the Safety, Device Performance and Possible Emergent Risks of Celotres in the Improvement of Wound Healing and the Resulting Scar Consequences Following Suturing of a Wound

Clinical Trial Summary

The objective of the study is to actively gather additional information on safety, device performance and possible emergent risks following the use of Celotres in a post-market setting when used to improve wound healing and the resulting scar consequences following suturing of a wound.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01706848
Study type Interventional
Source Halscion, Inc.
Contact
Status Completed
Phase N/A
Start date September 2012
Completion date May 2014
View Details
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