Trials / Completed
CompletedNCT04947202
Clinical Study on the Safety of SAFIL® MESH
Observational, Retrospective, Multi-center Clinical Study on the Safety of SAFIL® MESH in Patients Undergoing Reinforcement of Soft Tissues After Abdominal Wall Surgery or Other Fascial Defects
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 152 (actual)
- Sponsor
- Aesculap AG · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Observational, Retrospective, Multi-center Clinical Study on the Safety of SAFIL® MESH in Patients Undergoing Reinforcement of Soft Tissues After Abdominal Wall Surgery or Other Fascial Defects
Detailed description
The study design is a retrospective case-note series of patients that have undergone reinforcement of soft tissues with Safil® Mesh after abdominal wall surgery or other fascial defects between the period January 2019 - November 2020
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Hernioplasty | Hernioplasty is the repair of the defect using mesh patches. |
Timeline
- Start date
- 2021-07-01
- Primary completion
- 2021-11-30
- Completion
- 2021-11-30
- First posted
- 2021-07-01
- Last updated
- 2022-01-24
Locations
2 sites across 1 country: Spain
Source: ClinicalTrials.gov record NCT04947202. Inclusion in this directory is not an endorsement.