Trials / Completed
CompletedNCT04617041
Assessment of DAFILON® Suture Material for Skin Closure
Assessment of DAFILON® Suture Material for Skin Closure: A Prospective, Multicentric, International, Single-arm, Observational Study in Daily Practice
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 115 (actual)
- Sponsor
- Aesculap AG · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
In this non-interventional study (NIS) a polyamide non-absorbable suture (Dafilon®) will be evaluated for skin closure in adult and pediatric patients. The aim of the study is to collect clinical data on the performance of Dafilon® for skin closure. The results of this study will generate further clinical evidence for the use and the benefit of a non-absorbable surgical suture material produced from polyamide. Furthermore, the proactive collection of clinical data for Dafilon® suture will support the maintenance of the suture material on the market, so that in the future other patients can receive the suture material for skin closure.
Conditions
Timeline
- Start date
- 2021-03-11
- Primary completion
- 2023-05-25
- Completion
- 2023-06-15
- First posted
- 2020-11-05
- Last updated
- 2023-07-10
Locations
2 sites across 2 countries: Germany, Spain
Source: ClinicalTrials.gov record NCT04617041. Inclusion in this directory is not an endorsement.