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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

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

NCT number NCT03355001
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date January 3, 2018
Completion date September 21, 2019