Trials / Completed
CompletedNCT03355001
Prospective, International Monosyn® Quick - Non Interventional Study
Assessment of the Performance of Monosyn® Quick Suture Material in Different Indications Under Daily Clinical Routine.
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 153 (actual)
- Sponsor
- Aesculap AG · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
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
| Type | Name | Description |
|---|---|---|
| DEVICE | Monosyn® Quick | * Mucosal sutures in the facial and oral * Dermal sutures, particularly in pediatrics * Episiotomy * Circumcision |
Timeline
- Start date
- 2018-01-03
- Primary completion
- 2019-09-18
- Completion
- 2019-09-21
- First posted
- 2017-11-28
- Last updated
- 2022-01-11
Locations
3 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT03355001. Inclusion in this directory is not an endorsement.