A Preliminary, Non-comparative Study to Evaluate a Bioresorbable Wound Scaffold in Acute Wounds
NCT01081522 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12
Last updated 2010-03-05
Summary
As this is a proof-of-concept study, the primary objective is to provide preliminary data on the safety and efficacy of Bioresorbable Wound Scaffold in the management of acute wounds left to heal by secondary intent.
Conditions
- Pilonidal Sinus
Sponsors & Collaborators
-
ConvaTec Inc.
lead INDUSTRY
Principal Investigators
-
Dheerendra Kommala, MD · ConvaTec Inc.
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-10-31
- Primary Completion
- 2010-02-28
- Completion
- 2010-02-28
Countries
- Denmark
- United Kingdom
Study Locations
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