Clinical Trials Logo

Hernia, Inguinal clinical trials

View clinical trials related to Hernia, Inguinal.

Filter by:

NCT ID: NCT04211142 Recruiting - Hernia, Inguinal Clinical Trials

Pain and Quality of Life After Inguinal Hernia Repair: Laparoscopic Versus Open Repair.

QoL-TAPP
Start date: January 20, 2020
Phase: N/A
Study type: Interventional

This investigation will be a double-armed, randomized prospective study designed to compare open (Lichtenstein Technique) versus laparoscopic (TAPP) repair of primary unilateral inguinal hernia. Chronic pain, restriction of activities and esthetical outcome will be evaluated preoperatively and postoperatively, at 1, 4 and 12 months, using the European Registry for Abdominal Wall Hernias Quality of Life score (EuraHS-QoL score).

NCT ID: NCT04206956 Recruiting - Inguinal Hernia Clinical Trials

Anxiety and Chronic Postsurgical Pain Following Ambulatory Surgery in Children

ANXIDOU
Start date: October 14, 2019
Phase:
Study type: Observational

Prospective, monocentric, observationnal study. The primary objective of this study is to identify if presurgical child or/and parental anxiety is predictive of chronic postsurgical pain in abdominal or urologic ambulatory surgery.

NCT ID: NCT04203940 Completed - Inguinal Hernia Clinical Trials

Sutured Versus Cyanoacrylate Glue Mesh Fixation for Inguinal Hernia Repair

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

Because it avoids direct nerve irritation or entrapment, mesh fixation with tissue adhesive glue seems an optimal option to reduce postoperative pain. Indeed, preliminary results published with different glues all showed promising results with reduced postoperative pain. This randomized controlled study aimed to compare mesh fixation using N-butyl 2-cyanoacrylate with classical suture fixation in Lichtenstein hernia repair in terms of chronic groin pain, postoperative complications, operative time and recurrence.

NCT ID: NCT04171102 Completed - Inguinal Hernia Clinical Trials

Neo-nervegenesis in Inguinal Hernia Implant ProFlor

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

The investigation is aimed at specifically demonstrating the ingrowth of newly formed nervous elements within a 3D dynamic responsive implant for inguinal hernia repair.

NCT ID: NCT04149847 Not yet recruiting - Quality of Life Clinical Trials

Comparing the Quality of Life After Nylon Darn Repair of Inguinal Hernia to Polypropylene Mesh Repair

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Inguinal hernia repair may be done by the nylon darn, polypropylene mesh and other methods. Polypropylene mesh is established in the literature as the standard of care for inguinal hernia repair. It is however expensive and not readily available in our community hospitals. Nylon darn repair is widely used in our hospitals. We think that the quality of life following nylon darn repair and polypropylene mesh repair is similar. In order to find out, we are recruiting 79 patients to undergo nylon darn repair for their inguinal hernia and another 79 patients to undergo polypropylene mesh repair for their inguinal hernia repair. We are doing research to compare the quality of life after nylon darn repair of inguinal hernia to polypropylene mesh repair in patients aged 18 years to 80 years who come to St. Luke Hospital for their first-ever inguinal hernia repair.

NCT ID: NCT04131985 Completed - Postoperative Pain Clinical Trials

Analgesic Efficacy of Erector Spinae Plane Block for Laparoscopic Inguinal Hernia Repair

Start date: October 16, 2019
Phase: N/A
Study type: Interventional

Postoperative analgesia management in inguinal hernia surgery is difficult because of the content of the surgical procedure. A multimodal approach to postoperative analgesia has recently been proposed. For this reason, various methods are used.Regional blocks, pharmacological treatments are among these methods. Among the regional blocks, ilioinguinal and hypogastric blocks are used more safely and with increasing frequency, especially with the introduction of ultrasonography in the clinic.Forero et al. firstly, erector spinae block which was used for the first time in the treatment of thoracic neuropathic pain has been widely used especially in laparoscopic abdominal surgery and it has taken its place in the literature. It is performed at T4-5 level in breast and thoracic surgery and T7 level in abdominal surgery. In this block, local anesthesia between the erector spina muscle and the transverse protrusion of the vertebra was used to create analgesia in the anterior abdominal wall. In this study, we planned to investigate degree of postoperative pain, sensory block levels, analgesic consumption, propofol-remifentanyle consumption and side effects of patients undergoing inguinal hernia surgery under general anesthesia with erector spinae block.

NCT ID: NCT04114344 Active, not recruiting - Inguinal Hernia Clinical Trials

Clinical Trial to Compare TAPP (Transabdominal Preperitoneal) vs TEP (Totally Extraperitoneal) y Approach for Women's Inguinal Hernia on an Outpatient Basis

WOLAP
Start date: May 1, 2019
Phase: N/A
Study type: Interventional

Open prospective randomised clinical trial enrolling women who suffer from inguinal or femoral hernia, to evaluate if TEP approach is superior to TAPP concerning postoperative development, principally postoperative pain, with no increase of recurrent hernia at the one-year follow-up visit.

NCT ID: NCT04079504 Completed - Postoperative Pain Clinical Trials

Comparison of Postoperative Pain After Hernial Sac Ligation Versus Non-ligation in Inguinal Hernioplasty

Start date: October 1, 2019
Phase: N/A
Study type: Interventional

This study is intends to compare mean postoperative pain scores for 48-hours in patients undergoing Inguinal hernioplasty with and without hernia sac ligation in Department of Surgery, Dow University of Health Sciences & Dr. Ruth K. M. Pfau Civil Hospital Karachi.Half of the patients undergoing inguinal hernioplasty will have their indirect inguinal sacs ligated whereas other half will have non-ligation and inversion of sac.

NCT ID: NCT04074200 Recruiting - Inguinal Hernia Clinical Trials

Pain and Quality of Life After Inguinal Hernia Repair

PREPARE
Start date: August 26, 2019
Phase:
Study type: Observational

This study aims to explore the difference in outcomes relating to pain and quality of life after open, laparoscopic, and robotic-assisted inguinal hernia repair.

NCT ID: NCT04059640 Recruiting - Inguinal Hernia Clinical Trials

PMCF Study of LiquiBand FIX8® OHMF Device

LBF8-Open
Start date: December 7, 2021
Phase: N/A
Study type: Interventional

Study to evaluate the safety and performance of LiquiBand FIX8® Open Hernia Mesh Fixation Device.