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Assessment of DAFILON® Suture Material for Skin Closure

NCT04617041 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 115

Last updated 2023-07-10

No results posted yet for this study

Summary

In this non-interventional study (NIS) a polyamide non-absorbable suture (Dafilon®) will be evaluated for skin closure in adult and pediatric patients. The aim of the study is to collect clinical data on the performance of Dafilon® for skin closure. The results of this study will generate further clinical evidence for the use and the benefit of a non-absorbable surgical suture material produced from polyamide. Furthermore, the proactive collection of clinical data for Dafilon® suture will support the maintenance of the suture material on the market, so that in the future other patients can receive the suture material for skin closure.

Conditions

  • Laceration of Skin
  • Injury Skin

Sponsors & Collaborators

  • Aesculap AG

    lead INDUSTRY

Principal Investigators

  • Manuel Guillermo López Paredes, Dr. · Hospital Vall D'Hebrón, Barcelona

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-11
Primary Completion
2023-05-25
Completion
2023-06-15

Countries

  • Germany
  • Spain

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 NCT04617041 on ClinicalTrials.gov