Clinical Study on the Safety of SAFIL® MESH (SAFIL_MESH)

Aesculap

Status: Completed

Conditions: Fascial Hernia; Ventral Hernia; Abdominal Wall Defect; Abdominal Hernia

Treatments: Device: Hernioplasty

Study type: Observational

Funder types: Industry

Identifiers

NCT04947202

AAG-O-H-2040

Details and patient eligibility

About

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

Full 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

Enrollment: 152 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients operated between January 2019 - November 2020 for abdominal wall surgery or other fascial defects and received Safil® Mesh

Exclusion criteria

• No exclusion criteria have been set.

Trial design

152 participants in 1 patient group

Safil Mesh

Treatment:

Device: Hernioplasty