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PMCF-study Using Novosyn® Quick Suture Material for Skin Closure

NCT02680886 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2018-05-04

No results posted yet for this study

Summary

The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for skin closure. In order to show that, various safety and efficacy parameters have been selected. The outcome regarding these parameters will be evaluated by a quantitative summary of the available clinical data from the literature.

Conditions

  • Skin Closure

Interventions

DEVICE

Novosyn® Quick

Skin closure

Sponsors & Collaborators

  • B.Braun Surgical SA

    collaborator INDUSTRY

  • Aesculap AG

    lead INDUSTRY

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2017-10-31
Completion
2018-01-31

Countries

  • France
  • 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 NCT02680886 on ClinicalTrials.gov