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Clinical Study Into the Cosmetic Results of Leukosan Adhesive

NCT02179723 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 77

Last updated 2014-07-02

No results posted yet for this study

Summary

This clinical study aims to assess whether the benefits of using Leukosan Adhesive on trocar incisions are greater or equivalent to those provided by the standard therapy of transcutaneous sutures.

In particular, it tests the long-term cosmetic result after 3 months, the safety and tolerance, as well as the practicality of treatment with Leuksan Adhesive.

An open, randomised, controlled, prospective, single location, clinical study of women of ages between 18 and 60 years within the time span of March 2013 and April 2013.

Conditions

  • Wound Healing Cosmetic Result

Interventions

DEVICE

Leukosan Adhesive

Leukosan adhesive applied to one wound

DEVICE

Transcutaneous suture

Transcutaneous suture applied to one wound

Sponsors & Collaborators

  • Dr. Stephanie Krause

    lead INDUSTRY

Principal Investigators

  • Olaf Buchweitz, Priv.Doz. · Tagesklinik Altonaer Strasse

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2013-04-30
Completion
2013-07-31

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 NCT02179723 on ClinicalTrials.gov