NCT01622712View on ClinicalTrials.gov

Evaluation of Mesh Integration and Mesh Contraction After Open Preperitoneal Inguinal Hernia Repair Using a Memory Ring Containing Device

NACompletedINTERVENTIONAL
Enrollment

235

Participants

Timeline

Start Date

February 1, 2013

Primary Completion Date

September 2, 2014

Study Completion Date

September 2, 2014

Conditions
Unilateral Inguinal Hernia
Interventions
DEVICE

Rebound HRD Mesh

Patients with unilateral inguinal hernia receive a nitinol containing large pore polypropylene mesh.

Trial Locations (2)

9000

Ghent University Hospital, Ghent

9300

ASZ Aalst, Aalst

Sponsors

Collaborators (1)

Medri
All Listed Sponsors
collaborator

Medri

UNKNOWN

lead

University Hospital, Ghent

OTHER

NCT01622712 - Evaluation of Mesh Integration and Mesh Contraction After Open Preperitoneal Inguinal Hernia Repair Using a Memory Ring Containing Device | Biotech Hunter | Biotech Hunter