Optilene® Suture Material for Dermal Sutures

NCT05240248 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 172

Last updated 2024-02-21

No results posted yet for this study

Summary

In this non-interventional study, Optilene® suture will be evaluated for skin closure in adult patients.

Conditions

  • Laceration
  • Incision

Sponsors & Collaborators

  • B.Braun Surgical SA

    collaborator INDUSTRY
  • Aesculap AG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-22
Primary Completion
2023-06-23
Completion
2023-07-23

Countries

  • 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 NCT05240248 on ClinicalTrials.gov