11 results
Assessing the safety and efficacy of a new mesh (Parietex Composite Ventral Patch)
This study is a pilot study to examine the presence of antisperm antibodies after laparoscopic groin hernia repair in men. The hypothesis of this pilot study is: After laparoscopic groin hernia repair with a mesh, antisperm antibodies can be…
The objective of the International Hernia Mesh Registry is to observe a minimum of 3,500 patients for up to 2 years post implantation, in a post-market setting, following the use of either ETHICON Mesh Products or other marketed mesh products to…
The aim of this study is to evaluate the safety and the outcomes of laparoscopic correction of a recurrent inguinal hernia after previous repair.
Determine the effect of rectus femoris transfer on stroke survivors walking with a stiff knee gait on functional-, activity- and participation level.
The objective of this study is to determine whether early inguinal hernia repair (prior to discharge home) or late inguinal hernia repair (approximately 5 months after discharge home) is the safer surgical approach for premature infants who are…
The main objective is to asses functional anatomical restoration of the linea alba through functioning in mean peak torque, and ultrasound examination.
The aim of this study is to assess the efficacy of MR-HIFU as a treatment modality for desmoid-type fibromatosis (DTF).
The objective of this study is to collect additional data on the safety and performance of the slowly-resorbable TIGR® mesh in patients undergoing TEP for IGRP.
The objective of this study is to collect additional data on the performance and safety of the slowly-resorbable TIGR® mesh in patients undergoing TEP for IGRP. The study endpoints are described below.
The objective of this study is to collect additional data on safety and performance of Phasix* Mesh in subjects requiring VHWG Grade 3 midline hernia repair.