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Hernia, Inguinal clinical trials

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NCT ID: NCT03450811 Completed - Inguinal Hernia Clinical Trials

Effect of Inguinal Hernia Repair on Uroflowmetric Parameteres

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

Post operative acute urinary retension or voiding dysfunction are complications after inguinal hernia repair and they cause a great deal of discomfort and stress to patients. Furthermore, they can also increase hospital costs by increasing hospital stay, and by growing the need for outpatient appointments after an elective surgical procedure. Some studies recommend prophylactic alpha blockers to minimizing these adverse effects. Investigators aimed to determine the changes of uroflowmetric values for male patients following elective inguinal hernia repair.

NCT ID: NCT03411226 Completed - Clinical trials for Recurrent Inguinal Hernia

Feasibility of Re-TREPP in Patients With a Recurrent Inguinal Hernia After Previous TREPP Repair

re-TREPP
Start date: November 27, 2015
Phase: N/A
Study type: Observational

The Trans REctussheath PrePeritoneal (TREPP) mesh repair was introduced in 2006 to decrease the risk of postoperative inguinal pain in hernia surgery. For the repair of a recurrent inguinal hernia after a primary TREPP an alternative open anterior route (Lichtenstein) may seem the most logical option, but coincides with an increased risk of chronic postoperative inguinal pain. Therefore, this study aimed to evaluate the feasibility of a second TREPP procedure to repair a recurrent inguinal hernia after an initial TREPP repair. The hypothesis was that the technique is possible and does not lead to an increased risk of postoperative pain.

NCT ID: NCT03392636 Completed - Hernia, Inguinal Clinical Trials

Comparison of Recurrence Rate of 2 Herniotomy Techniques in Children Older Than 2 Years

Start date: November 11, 2016
Phase: N/A
Study type: Interventional

the study is basically aimed at comparing two techniques of herniotomy by comparing there recurrence rates

NCT ID: NCT03352362 Completed - Inguinal Hernia Clinical Trials

Comparison of the Effect of Propacetamol, Ibuprofen or Their Combination on Postoperative Pain and Quality of Recovery After Laparoscopic Hernia Repair in Children

Start date: December 15, 2017
Phase: N/A
Study type: Interventional

There are difficulties in the progress of the study and cancel the plan. The purpose of this study is to evaluate the postoperative pain control using non - opioidal analgesics in children. The investigators will investigate the effect of single use and combination of caldorol(ibuprofen) compare to denogan(propacetamol) in children. Participants who receive the laparoscopic inguinal hernia repair between 6 months and 6 years old are divided 3 groups(caldolor, denogan, combination). Each groups are received a medication by protocol during surgery. After operation patient's pain score and use of additional analgesics are recorded in postanesthesia care unit and general ward.

NCT ID: NCT03326700 Completed - Sexual Dysfunction Clinical Trials

Effects of Hernia Repair on Men's Sexual Functions

Start date: November 2015
Phase: N/A
Study type: Interventional

In the literature, there are several studies that compare Laparoscopic totally extraperitoneal hernia repair (TEP) with Lichtenstein hernia (LH) repair. There are no studies that compare sexual functions on men's health and quality of life. Our aim was to study the sexual functions of men, who underwent TEP or LH repair according to Health Survey Scoring Demonstration (SF36) and The International Index of Erectile Function (IIEF).

NCT ID: NCT03276871 Completed - Inguinal Hernia Clinical Trials

Telescopic Dissection vs. Balloon Dissection During Laparoscopic TEP Inguinal Hernia Repair

Start date: August 28, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the surgical technique for creation of extraperitoneal space during laparoscopic TEP inguinal hernia repair (telescopic dissection or balloon dissection) has an impact on operative times, early postoperative pain scores, surgical complications and rate of hernia recurrence following laparoscopic TEP inguinal hernia repair.

NCT ID: NCT03247985 Completed - Hernia, Inguinal Clinical Trials

Tacking Mesh Versus Self-fixating Mesh for Inguinal Hernia Repair

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

Investigators are testing whether tacking mesh or self-fixating mesh used for inguinal hernia repair makes any difference in short-term pain or return to normal activities following the operation. Other studies have shown no significant difference in hernia recurrence rate when metal tacks are not used to hold the mesh in place.

NCT ID: NCT03221686 Completed - Inguinal Hernia Clinical Trials

Effects of Oral Supplementation of Arginine, Zinc and Vitamin C on Collagen Synthesis in Inguinal Hernia Patients

Start date: February 20, 2016
Phase: N/A
Study type: Interventional

Collagen synthesis is depressed systemically in the immediate postoperative period. Arginine, zinc and vitamin C impact collagen synthesis. The aim of this study is to investigate the effect of a pre and postoperative oral supplement consisting of arginine, zinc and vitamin C on collagen synthesis in patients undergoing inguinal hernia repair.

NCT ID: NCT03203343 Completed - Surgery Clinical Trials

Inflammatory Stress Response in Pediatric Inguinal Hernia Repair

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Today there are various surgical techniques for inguinal hernia. In this study, investigators want to compare the ''PIRS'' operating technique laparoscopy and modified "Marcy" operating technique with open inguinal access. Investigators would compare both groups to find out witch one does the lesser inflammatory stress response on the organism.

NCT ID: NCT03193723 Completed - Inguinal Hernia Clinical Trials

Ultrasound Guided Local Anesthetic Field Block (A Five Step Procedure) for Open Inguinal Hernia Repair

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate success, efficacy, feasibility and safety of a simple five step ultrasound guided local anesthetic infiltration technique for unilateral open inguinal hernia repair and to determine the non-inferiority of the block to spinal anesthesia by comparing intraoperative and postoperative complications, pain control and patient and surgeon satisfaction of the block with spinal anesthesia.