NCT00827944 - Parietex Progrip Study | Biotech Hunter

Enrollment

603

Participants

Timeline

Start Date

October 31, 2008

Primary Completion Date

October 31, 2012

Study Completion Date

October 31, 2012

Conditions

Hernia, Inguinal

Interventions

DEVICE

Parietex Progrip

"Surgical technique:~Self-gripping lightweight Polyester and Polylactic acid meshes providing a sutureless fixation."

DEVICE

Low weight polypropylene mesh

"Surgical technique:~Lichtenstein repair with lightweight polypropylene mesh (inferior to 70gr/m2) secured to the posterior inguinal wall with sutures"

Trial Locations (9)

3000

Universitaire Ziekenhuizen Leuven, Leuven

28177

Klinikum Bremen-Mitte, Bremen

D- 36039 Fulda

Herz-Jesu-Krankenhaus gGmbH, Chirurgische Klinik, Fulda

5623 EJ

Catharina-ziekenhuis, Eindhoven

582 24

Medical Center Linköping, Linköping

721 89

Centre of clinical research, Västeras-

G11 6NT

Western Infirmary, Glasgow

W2 1NY

Imperial College London / Faculty of Medecine, London

PL6

Derriford Hospital, Plymouth