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Hernia clinical trials

View clinical trials related to Hernia.

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NCT ID: NCT03421925 Not yet recruiting - Hernia, Inguinal Clinical Trials

Effects of Using Divided Mesh and Using a Non Divided Mesh on Testicular Blood Flow and Volume in Laparoscopic Hernia Repair

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Laparoscopic inguinal hernia repair techniques has been compared with the open techniques in several studies. However, no one studied about the different uses of the same type of mesh on the same surgical technique, and effects of this different use on testicular volume and blood flow. The objective of this study is to investigate the effects at 6 months of the divided and non divided mesh in laparoscopic totally extraperitoneal hernia repair technique on testicular volume and blood flow by use of Doppler Ultrasonography

NCT ID: NCT03359564 Not yet recruiting - Clinical trials for Lumbar Disc Herniation

Microendoscopic Lumbar Discectomy: A Study of 100 Cases

Start date: January 1, 2018
Phase: N/A
Study type: Observational

Evaluate the outcome of micro endoscopic discectomy (MED) by tubular retractors on safety and efficacy of the technique.

NCT ID: NCT03314259 Not yet recruiting - Inguinal Hernia Clinical Trials

Prophylactic Alpha-blockers in the Prevention of Urinary Retention Post Inguinal Hernia Repair

Start date: December 1, 2017
Phase: Early Phase 1
Study type: Interventional

Post operative urinary retention ( POUR) is caused by sympathetic activation of the internal urethral sphincter after surgery. The smooth muscles of the around the internal urethral sphincter have been demonstrated to be rich in alpha-1 adrenergic receptors. Our research idea is novel because there has been no prior prospective study conducted using alpha-blockers to reduce post-operative urinary retention in patients undergoing inguinal hernia repair. The proposed research is important as existing studies that sought to understand POUR have merely established the risks factors involved. Despite so, the incidence of POUR remains high and no studies to date have investigated the use of specific interventions to reduce the risk of POUR. This is essential as patients who develop POUR have also been successfully shown to have significantly longer length of hospitalisation. Besides, the development of POUR can also cause significant pain/discomfort, increase risks of long-term urethral catheterisation and predispose patients to urinary tract infections

NCT ID: NCT03128216 Not yet recruiting - Inguinal Hernia Clinical Trials

Local Anesthetic Infiltration VS Trasversalis Fascia Block VS Spinal Anesthesia

Start date: April 2017
Phase: N/A
Study type: Interventional

Propose to comparison effectiveness of blind local anesthetic infiltration with ultrasound guided Transversals Fascia Block and Spinal Anesthesia in patients undergoing to inguinal hernia repair surgery. The effectiveness is defined as pain control during intraoperative and time need to reach hospital discharge criteria in the post-operative period.

NCT ID: NCT02932033 Not yet recruiting - Inguinal Hernia Clinical Trials

Trial Comparing Tack Versus Histoacryl Mesh Fixation After Endoscopic TEP(Total Extraperitoneal) Repair for Bilateral Inguinal Hernia

TEP
Start date: November 2016
Phase: N/A
Study type: Interventional

This prospective randomized trial is performed to analyze the post-operative pain (acute and chronic) after endoscopic TEP repair after bilateral inguinal hernia repair.

NCT ID: NCT02928146 Not yet recruiting - Inguinal Hernia Clinical Trials

Lichtenstein Versus TAPP and TEP in Groin Hernioplasty

TAPP&TEP
Start date: January 2017
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the effectiveness of various methods of inguinal hernia repair and to evaluate techniques of synthetic mesh fixation during laparoscopic and open hernia repair.

NCT ID: NCT02896686 Not yet recruiting - Incisional Hernia Clinical Trials

Efficacy of an Onlay Mesh for Prevention of Incisional Hernia After Loop Ileostomy Closure

ILEOMESH
Start date: October 2016
Phase: Phase 4
Study type: Interventional

The aim of the present study is to determine the efficacy of the placement of an onlay mesh to prevent incisional hernia after loop ileostomy closure in patients with a prior rectal resection for cancer

NCT ID: NCT02788812 Not yet recruiting - Inguinal Hernia Clinical Trials

QOL in Incarcerated Inguinal Hernias: TAPP Vs Open Repair

Start date: June 2016
Phase: N/A
Study type: Interventional

To determine if there is a difference in the quality of life in between patients who undergoes laparoscopic transabdominal pre-peritoneal (TAPP) or modified Lichtenstein hernioplasty

NCT ID: NCT02358291 Not yet recruiting - Clinical trials for Lumbar Disc Herniation

Microendoscopic Discectomy Vs Transforaminal Endoscopic Lumbar Discectomy Vs Open Discectomy

Start date: March 2015
Phase: Phase 1/Phase 2
Study type: Interventional

In our study, a multicenter randomized controlled,single blind trial will be performed to evaluate the effectiveness and safety of these three procedures for the treatment of symptomatic lumbar disc herniation.

NCT ID: NCT02292095 Not yet recruiting - Inguinal Hernia Clinical Trials

Effects of Transverse Abdominis Plane Block Guided by Ultrasound on the Postoperative Analgesia and Quality of Lives Among the Patients Undergo Inguinal Hernia Repair

Start date: January 2016
Phase: Phase 4
Study type: Interventional

The incidence of post-operative pain after open inguinal hernia repair is high and impair the quality of lives of the patients.The purpose of this study is to determine whether transverse abdominis plane block combined with intravenous patient controlled analgesia is superior to intravenous patient controlled analgesia in improving the quality of life and reducing the incidence of chronic post-surgical pain