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Hernia, Inguinal clinical trials

View clinical trials related to Hernia, Inguinal.

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NCT ID: NCT02302937 Completed - Clinical trials for Primary Unilateral Inguinal Hernia

SIngle Port vs Standard TEP for Primary Inguinal Hernia Repair

LESSTEP
Start date: August 2011
Phase: N/A
Study type: Interventional

This study is carried out to determine if laparoscopic inguinal TEP repair of the hernia using a mesh carried out with only 1 port (hole) results in the reduction of post- operative pain and use of painkillers, shorter hospital stay and lesser complications than that carried out using conventional 3 ports.

NCT ID: NCT02240550 Completed - Inguinal Hernia Clinical Trials

A Comparative Clinical Study to Evaluate the Effectiveness of ProFlor vs. Lichtenstein for Inguinal Hernia Repair

Start date: September 2014
Phase: N/A
Study type: Interventional

This investigation will be a double-armed, randomized (Blinded patients and Blinded examiner) prospective study designed to collect perioperative and postoperative data to compare the QOL of ProFlor vs. Lichtenstein inguinal hernia repair.

NCT ID: NCT02239185 Completed - Clinical trials for Congenital Inguinal Hernia

Laparoscopic Inguinal Hernia Repair in Infancy and Childhood

LIHR-2014
Start date: May 2012
Phase: N/A
Study type: Interventional

Aim of the study The aim of this study is to test the hypothesis that during laparoscopic hernia repair, disconnection of the hernial sac along with suture ligation of the neck is better than transperitoneal purse string suture around the hernial sac at the neck leaving the sac in continuity. Also to compare the two different laparoscopic techniques as regards operative time, recurrence rate, hydrocele formation, and other possible complications as bleeding, hematoma, injury of the vas and testicular atrophy and post-operative cosmetic results. ..

NCT ID: NCT02210416 Completed - Inguinal Hernia Clinical Trials

Costs of Complications in Inguinal Hernia Repair

Start date: December 2012
Phase: N/A
Study type: Observational

Laparoscopic inguinal hernia repair is becoming increasingly popular mainly because of short-term advantages compared to open hernioplasties with mesh. In the prevailing economic climate, the total costs of treatment is a subject of intense research. This study is designed to evaluate the results of open and laparoscopic inguinal hernia repairs, with a special emphasis in costs of treatment, complications and convalescence.

NCT ID: NCT02197585 Completed - Chronic Pain Clinical Trials

Comparison of Mesh Fixation Wit Cyanoacrylate vs Suture in Inguinal Hernia Surgery

UHU
Start date: June 2007
Phase: N/A
Study type: Interventional

To compare fixation with glubran2 with suture during surgery por primary inguinal hernia. Hypothesis: Glue may induce less complications and chronic pain than suture

NCT ID: NCT02110745 Completed - Hernia, Inguinal Clinical Trials

The Effect of Induction Technique on Postoperative Pain and Agitation

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The objective of this study was to determine (a) whether patients anesthetized with intravenous propofol have less pain compared with sevofluorane for paediatric inguinal hernia and undescended testis operations and (b) whether intravenous propofol anesthesia has better quality of recovery compared with sevofluorane anesthesia in the immediate postoperative period after paediatric inguinal hernia and undescended testis operations.

NCT ID: NCT02065219 Completed - Chronic Pain Clinical Trials

Trigger-point Blockade in Persistent Pain After Open Groin Hernia Repair

Trigger-open
Start date: November 2013
Phase: Phase 3
Study type: Interventional

Groin hernia repair is a common procedure performed in approximately 2,000 patients per one million inhabitants. Severe chronic pain following groin hernia repair is seen in 2-5% of the patients indicating that a large number of patients each year suffer from debilitating reduction in health-related quality of life. This study examines the effect of ultra-sound guided blocks with local anesthesia in the groin in regard to pain relief and sleep quality. The hypothesis of the study is that a block will confer significant pain relief to patients with severe chronic pain following open groin hernia repair.

NCT ID: NCT02062775 Completed - Inguinal Hernia Clinical Trials

Comparison of Self-Fixating vs Non-Fixating Hernia Mesh

Start date: August 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if self-fixating polyester mesh will have lower incidence of chronic postoperative pain and recurrence than non-fixating polyester mesh when used for laparoscopic inguinal hernia repair.

NCT ID: NCT02055053 Completed - Clinical trials for Post Operative Pain (Post Laparoscopic Hernia Repair)

Effects of Local Anesthesia on Post-operative Pain During Laparoscopic Inguinal Hernia Repair

Start date: August 2013
Phase: Phase 4
Study type: Interventional

To assess effect of local anesthetic into the preperitoneal space during laparoscopic hernia repair on post-operative pain.

NCT ID: NCT02049255 Completed - Pain Clinical Trials

Comparision of the Use in Marcaine and Chloroprocaine in Rachianesthesia for the Surgical Correction of Inguinal Hernia.

Start date: November 2013
Phase: Phase 4
Study type: Interventional

Comparison the use of marcaine and chloroprocaine in rachianesthesia for a surgical correction of inguinal hernia. Comparision between acute and chronic (3 months and 6 months) pain.