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Clinical Outcome of Defect Reconstruction Using IDRT Single Layer : Results From a Prospective Multicentric Trial

NCT01704950 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 52

Last updated 2016-02-25

No results posted yet for this study

Summary

The aim of this study is to provide data and the guidelines for the use of IDRT SL in small wounds, acute and chronic (less than 6 months), showing the benefits and the easy to use of this product as a one stage procedure.

Conditions

  • Traumatic Wound
  • Reconstruction Wound

Sponsors & Collaborators

  • Integra LifeSciences Services

    lead INDUSTRY

Principal Investigators

  • Stefanos Papadopoulos · General State Hospital of Athens, "G. Gennimatas"

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2014-07-31
Completion
2015-08-31

Countries

  • Germany
  • Greece
  • Italy
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01704950 on ClinicalTrials.gov