Trials / Completed
CompletedNCT02680886
PMCF-study Using Novosyn® Quick Suture Material for Skin Closure
Post-Marketing Clinical Follow-up (PMCF) Study for Skin Closure to Evaluate the Safety and Efficacy of Novosyn® Quick Suture Material. A Multicenter, International, Prospective, Observational Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (actual)
- Sponsor
- Aesculap AG · Industry
- Sex
- All
- Age
- 1 Year
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for skin closure. In order to show that, various safety and efficacy parameters have been selected. The outcome regarding these parameters will be evaluated by a quantitative summary of the available clinical data from the literature.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Novosyn® Quick | Skin closure |
Timeline
- Start date
- 2016-03-01
- Primary completion
- 2017-10-01
- Completion
- 2018-01-01
- First posted
- 2016-02-12
- Last updated
- 2018-05-04
Locations
2 sites across 2 countries: France, Germany
Source: ClinicalTrials.gov record NCT02680886. Inclusion in this directory is not an endorsement.