Clinical Experience With a Tensor Fasciae Latae Perforator Flap Based on Septocutaneous Perforators

This study has been completed.
Sponsor:
Information provided by:
Medical University of Graz
ClinicalTrials.gov Identifier:
NCT01136044
First received: May 28, 2010
Last updated: June 2, 2010
Last verified: June 2010
  Purpose

The purpose of this study is to evaluate the possible harvest of a tensor fasciae latae flap based on septocutaneous perforators.This study should further confirm our data from an anatomical study concerning location, distribution, diameter and differentiation of the perforators.


Condition Intervention
Soft Tissue Defect
Other: septocutaneous perforator flap

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Clinical Experience With a Tensor Fasciae Latae Perforator Flap Based on Septocutaneous Perforators

Further study details as provided by Medical University of Graz:

Primary Outcome Measures:
  • Confirmation of the anatomical data in the clinical trial [ Time Frame: January 2008 till may 2010 ] [ Designated as safety issue: No ]
    Since the purpose of this study was to confirm our anatomical data in a clinical trial, the location, the differentiation and the diameter of the septocutaneous perforators has been measured and recorded during flap elevation.


Enrollment: 14
Study Start Date: January 2008
Study Completion Date: May 2010
Primary Completion Date: February 2010 (Final data collection date for primary outcome measure)
Intervention Details:
    Other: septocutaneous perforator flap
    Perforator flaps can be based on septocutaneous or musculocutaneous perforators. If septocutaneous perforators are present, the harvest of these flaps is more straight forward and the dissection of the pedicle is easy.
    Other Names:
    • fasciocutaneous flaps
    • perforator flap
  Eligibility

Ages Eligible for Study:   16 Years to 71 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • soft tissue defect
  • no previous operations in the thigh region

Exclusion Criteria:

  • obese patients
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01136044

Locations
Austria
Department of Surgery, Division of Plastic Surgery
Graz, Austria, 8010
Sponsors and Collaborators
Medical University of Graz
Investigators
Principal Investigator: Martin Hubmer, MD Medical University of Graz
  More Information

Publications:
Responsible Party: Dr.Martin Hubmer, Medical University of Graz
ClinicalTrials.gov Identifier: NCT01136044     History of Changes
Other Study ID Numbers: MUG111
Study First Received: May 28, 2010
Last Updated: June 2, 2010
Health Authority: Austria: Ethikkommission

Keywords provided by Medical University of Graz:
tensor fasciae latae
septocutaneous perforators

ClinicalTrials.gov processed this record on July 23, 2014