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Prospective, International Monosyn® Quick - Non Interventional Study

NCT03355001 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 153

Last updated 2022-01-11

No results posted yet for this study

Summary

The Monosyn® Quick non-interventional study (NIS) has been designed to implement an action within the framework of a proactive post-market surveillance system.

The aim of this NIS is to collect systematically and proactively different clinical parameters regarding safety, effectiveness and performance of Monosyn® Quick suture material under the daily clinical practice when used as intended.

Conditions

  • Pediatric and Adult: Mucosal Closure in Facial and Oral Surgery
  • Pediatric and Adult: Skin Closure (Dermal Sutures)
  • Women: Episiotomy
  • Pediatric: Urological Interventions (Circumcision, Phimosis Etc.)

Interventions

DEVICE

Monosyn® Quick

* Mucosal sutures in the facial and oral * Dermal sutures, particularly in pediatrics * Episiotomy * Circumcision

Sponsors & Collaborators

  • B.Braun Surgical SA

    collaborator INDUSTRY

  • Aesculap AG

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-03
Primary Completion
2019-09-18
Completion
2019-09-21

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 NCT03355001 on ClinicalTrials.gov