Viewing Study NCT04358159


Ignite Creation Date: 2025-12-24 @ 3:02 PM
Ignite Modification Date: 2026-01-01 @ 4:00 PM
Study NCT ID: NCT04358159
Status: RECRUITING
Last Update Posted: 2025-08-13
First Post: 2020-04-19
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: RCT Ventralex vs Onlay Mesh in Incisional Hernias
Sponsor: Karolinska Institutet
Organization:

Study Overview

Official Title: Randomised Controlled Trial of Ventralex Versus Onlay Mesh Repair for Midline Incisional Hernias
Status: RECRUITING
Status Verified Date: 2025-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: VPatchIncRCT
Brief Summary: A radomised controlled trial comparing Ventralex patch and Progrip mesh in surgery for midline incisional hernias
Detailed Description: Incisional hernias in the midline is among the most common conditions requiring surgery. There are several factors which can increase the risk of incisional hernias, e.g. surgical technique, truncal obesity and other co-morbidities.

Repair with mesh-reinforcement is considered standard for the treatment of incisional hernias. Onlay and sublay mesh placements are the most commonly used methods. There are many different types of mesh available to use. Despite the widely use of composite ventral-patch Ventralex, there are few studies with small numbers of patients showing the advantage and disadvantage of ventral-patch. Some studies show that the onlay mesh-reinforcement remains a good alternative to the sublay mesh technique, while others showing fewer recurrences with the sublay mesh technique. The Ventralex mesh is usually placed on the peritoneum as a Intra peritoneum onlay mesh (IPOM). In this study intend to compare pre peritoneal Ventralex® mesh in sublay position with ProGrip self-fixating onlay mesh.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: