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Flap Preconditioning by Intermittent Negative Pressure

NCT03900065 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2019-04-02

No results posted yet for this study

Summary

A randomized controlled trial to investigate the effect of negative pressure preconditioning of flaps on surgical outcome and microcirculation of the tissue.

Conditions

  • Complication of Surgical Procedure
  • Flap Ischemia

Interventions

PROCEDURE

Preconditioning

Foam-mediated intermittent negative pressure will be applied to the skin of the planned flap for 5 days before surgery.

Sponsors & Collaborators

  • Ruhr University of Bochum

    lead OTHER

Principal Investigators

  • Björn Behr, MD · Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil Bochum

  • Mehran Dadras, MD · Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil Bochum

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2020-06-01
Completion
2020-07-01

Countries

  • Germany

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 NCT03900065 on ClinicalTrials.gov