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Hernia, Inguinal clinical trials

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NCT ID: NCT00960011 Completed - Hernia, Inguinal Clinical Trials

Comparative Study on Self-adhesive Mesh for Open Inguinal Hernia Repair

Start date: June 2009
Phase: N/A
Study type: Interventional

Tension-less mesh repair is the most common procedure for inguinal hernia. Conventional heavy weight polypropylene meshes have been reported to stimulate inflammatory reaction and this is responsible for mesh shrinkage and postoperative chronic groin pain. Moreover, the fixation of the mesh with sutures is a tedious procedure and accounts for the majority of the operating time. A self gripping semi-absorbable mesh has been developed for anterior tension free inguinal hernia repair. It has the benefit of light weight property and does not require sutures for fixation. This study aims to compare the outcome of this self-gripping light weight mesh with the conventional heavy weight polypropylene mesh in inguinal hernia repair.

NCT ID: NCT00941941 Unknown status - Hernia, Inguinal Clinical Trials

Non-Mesh Versus Mesh Method for Inguinal Hernia Repair

IHR
Start date: May 2009
Phase: N/A
Study type: Interventional

The study aims at establishing the effectiveness of the non-mesh (Desarda) technique for the treatment of primary inguinal hernias at Mulago Hospital in Uganda. First developed and used in India, the Desarda method is reported to offer superior outcomes such as minimal postoperative groin pain and near zero recurrence rates. In comparison to the mesh-based repairs, it is a simple and affordable technique suitable for the resource-constrained communities. It is devoid of complications associated with foreign body implants. Early clinical outcomes which include acute groin pain, time to resumption of normal gait, operative time and complications will be assessed. Participants will be followed at 2 hours, 3 days, 7 days and 14 days postoperatively. The investigators hypothesize that the mean postoperative acute groin pain score, or the mean postoperative day of return to normal gait is different in adult patients who undergo the non-mesh (Desarda) repair from what it is in those who undergo the mesh (Lichtenstein) technique of hernia repair.

NCT ID: NCT00940433 Completed - Inguinal Hernia Clinical Trials

Hernia Repair Four Arm Comparative Study

Start date: February 2008
Phase: N/A
Study type: Interventional

This study compares the outcome of the four most commonly used operations for the repair of primary groin hernia including the new key hole surgical techniques. It aims at answering the question of whether the new technology really improve the outcome, saves time and reduce patient suffering.

NCT ID: NCT00925067 Completed - Inguinal Hernia Clinical Trials

Effects of Lightweight Meshes in Laparoscopic Inguinal Hernia Repair on Quality of Life and Male Fertility Aspects

Start date: April 2003
Phase: N/A
Study type: Interventional

A randomized, prospective clinical trial analyzing whether the use of lightweight prostheses during laparoscopic inguinal hernia repair of male patients could have a beneficial effect on postoperative discomfort, chronic pain development, recurrence and male fertility aspects.

NCT ID: NCT00924755 Unknown status - Hernia, Inguinal Clinical Trials

Study of Surgical Mesh for Inguinal Hernia Repair

Start date: June 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the early outcomes when using the Biomerix Reviveā„¢ as a tension-free onlay patch, Lichtenstein-style, in patients who are candidates for primary, unilateral, open inguinal hernia repair.

NCT ID: NCT00827944 Completed - Hernia, Inguinal Clinical Trials

Parietex Progrip Study

Start date: October 2008
Phase: Phase 4
Study type: Interventional

The objective of the study is to evaluate pain and disabling complications inducing social consequences in primary inguinal hernia ProGrip mesh repair compared to Lichtenstein repair with lightweight polypropylene mesh.

NCT ID: NCT00825344 Completed - Postoperative Pain Clinical Trials

Preoperative Etanercept Before Inguinal Hernia Surgery

Start date: January 2009
Phase: N/A
Study type: Interventional

Inguinal hernia repair is one of the most frequently performed operations in young men. Persistent pain after inguinal surgery represents a significant cause of disability, occurring in between 15%-35% of cases. In a majority of these patients, their groin pain persisted after a previous hernia repair. The main type of chronic postsurgical pain is neuropathic, caused by injured nerves. One of the principal components in the pathophysiology of postsurgical pain is cytokines, specifically tumor necrosis factor (TNF). In animal studies, injecting TNF inhibitors before nerve injury can reduce pain behaviors and neuropathology. Finding a way to reduce the incidence of postsurgical pain after hernia repair could enhance function, and reduce the need for opioids and other analgesics. The investigators intend to conduct the first randomized, controlled study evaluating whether preemptive administration of a tumor necrosis inhibitor can reduce postoperative pain and opioid consumption after hernia repair. This is important because the degree and intensity of postsurgical pain is a major predictor for the development of chronic postsurgical pain.

NCT ID: NCT00820131 Completed - Chronic Pain Clinical Trials

Chronic Pain After Inguinal Hernia Repair

GRIP-ME
Start date: January 2008
Phase: Phase 4
Study type: Interventional

Chronic pain after inguinal hernia repair has become a major concern. Although tension-free Lichtenstein technique is used and new lightweight meshes have been developed, still up to 40 % of patients complain of some kind of pain even one year after surgery. The necessity of mesh-fixation using sutures, could be causative. However, current data do not provide evidence whether suture fixation in Lichtenstein repair might be the reason for chronic postoperative pain. A newly developed selfgrip-mesh enables sutureless fixation of the mesh in open inguinal hernia repair. Hereby a polypropylene mesh is combined with a resorbable polylactic-acid gripping system. Thereby the rate of chronic postoperative pain could be decreased. Two techniques of inguinal hernia repair will be evaluated: 1. open anterior mesh repair using conventional Lichtenstein technique (sutures for mesh-fixation) 2. open anterior mesh repair using a selfgrip mesh (polylactic-acid gripping system for mesh fixation) Postoperative pain will be evaluated by visual analog scale and Mc Gill pain questionaire at the 10th day, as well as 3 and 15 months postoperatively.

NCT ID: NCT00815698 Completed - Inguinal Hernia Clinical Trials

Effect of Suture for Mesh Fixation in Lichtenstein Hernia Repair

Dangrip
Start date: December 2008
Phase: N/A
Study type: Interventional

The investigators want to evaluate the effect of suturing the mesh versus using a self-adhesive mesh for Lichtenstein hernia repair. Effect parameters include chronic pain.

NCT ID: NCT00793286 Completed - Pain Clinical Trials

Stapler Versus Glue for Laparoscopic Groin Hernia Repair

Start date: August 2004
Phase: N/A
Study type: Interventional

Repair of inguinal hernia is the most common operation of the general surgeon. In recent years, it was recognized that chronic postoperative pain is as important for postoperative outcome as recurrent hernia. The incidence of pain or discomfort ranges up to 60% of operated patients. Despite the fact that laparoscopic hernia repair has been shown to reduce postoperative pain compared to open hernia repair, up to 5% of patients suffer from persistent discomfort. During that operation the mesh is either fixed using a stapler or tissue adhesive glue. With the current study we compare postoperative pain between patients undergoing laparoscopic inguinal hernia repair with either mesh fixation using a stapler or tissue adhesive. The use of von Frey monofilaments allows to describe pain with a high sensitivity.