Clinical Experience With a Tensor Fasciae Latae Perforator Flap Based on

Clinical Trial Summary

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.

See also
	Status	Clinical Trial	Phase
	Completed	`NCT01871103` - The Dorsal Homodigital Island Flap Based on the Dorsal Branch of the Digital Artery: A Review of 171 Cases	N/A
	Active, not recruiting	`NCT04703738` - Evaluation of Geistlich Fibro-Gide® in Comparison to CTG for the Treatment Around Implants	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01871103 - The Dorsal Homodigital Island Flap Based on the Dorsal Branch of the Digital Artery: A Review of 171 Cases

N/A

Active, not recruiting

NCT04703738 - Evaluation of Geistlich Fibro-Gide® in Comparison to CTG for the Treatment Around Implants

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01136044
Study type	Interventional
Source	Medical University of Graz
Contact
Status	Completed
Phase	N/A
Start date	January 2008
Completion date	May 2010

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms