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Hernia clinical trials

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NCT ID: NCT02336256 Completed - Inguinal Hernia Clinical Trials

Plasma Total Antioxidant Status and Thiobarbituric Acid-reacting Substances in Patients With Inguinal Hernia

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

Introduction: Any form of trauma, including surgery is known to result in oxidative stress. Single incision laparoscopy is a step forward towards almost scarless surgery. It is also expected to result in a lower degree of free radicals generation and faster normalization of the organism's antioxidant capacity. Aim: The aim of the study was to assess a number of plasma oxidative stress markers in patients operated due to inguinal hernia using typical totally extra peritoneal (TEP) and modified single incision laparoscopic surgery (SILS) methods. Material and methods: Thirty-two consecutive patients with no acute disease and severe chronic disorder, were qualified for inguinal hernia laparoscopic surgery. All were caucasian males, aged 24-69 and they underwent one of two surgical approaches: totally extra-peritoneal repair (TEP) and single incision laparoscopic surgery (SILS). TEP patients created Group 1 (n= 17) and SILS patients formed Group 2 (n= 17). Total antioxidant status (TAS) and thiobarbituric acid-reacting substances (TBARS) were determined in three time points: before, one day and four days after the laparoscopic surgery.

NCT ID: NCT02329938 Completed - Inguinal Hernia Clinical Trials

Desarda Repair for Inguinal Hernia

Start date: December 2010
Phase: N/A
Study type: Interventional

Unlike Lichtenstein tension free repair for inguinal hernia, Desarda's repair was introduced as a pure tissue repair with no need for mesh. In other words; the complications which may arise from the use of a foreign body (mesh) will be avoided. The idea was to evaluate the efficacy of this new repair and compare it to the standard Lichtenstein repair.

NCT ID: NCT02321059 Completed - Incisional Hernia Clinical Trials

Validation of the Goodstrength System for Assessment of Abdominal Wall Strength in Patients With Incisional Hernia

VAGSI
Start date: November 2014
Phase: N/A
Study type: Observational

Patients with an incisional hernia in the midline and controls with an intact abdominal wall are examined twice with one week apart, in order to establish the test-retest reliability and internal and external validity of the Goodstrength trunk dynamometer.

NCT ID: NCT02314091 Completed - Incisional Hernia Clinical Trials

Long Term Results of Randomized Prospective Comparison of Onlay and Sublay Mesh Repair Techniques for Incisional Hernia

IH01
Start date: January 2011
Phase: N/A
Study type: Interventional

Randomised prospective comparison of onlay and sublay mesh repair techniques in incisional hernia

NCT ID: NCT02310958 Completed - Hernia, Inguinal Clinical Trials

Outcome of Laparoscopic Inguinal Herniorraphy in Children

Start date: March 2010
Phase:
Study type: Observational

The investigators plan a retrospective, single-center outcome analysis of laparoscopic hernia repair in children operated between March 2nd, 2010, and March 1st, 2014. Data analysis will be based on a review of hospital records and a questionnaire answered by families. Patient demographics (age, gender), affected side, type and duration of laparoscopic intervention, and outcome parameters (hernia recurrence, post-operative complications, eg. infections, length and type of postoperative pain medication, and length of the postoperative hospital stay) will be analysed.

NCT ID: NCT02305082 Completed - Hernia, Ventral Clinical Trials

Fast-track Giant Ventral Hernia Repair

Start date: December 2014
Phase: N/A
Study type: Observational

The implementation of an enhanced recovery pathway after giant ventral hernia repair, including preoperative high-dose steroid is examined prospectively and compared with a group of historic controls.

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: NCT02297711 Completed - Hernia Clinical Trials

TEP Versus Open Minimal Suture Repair for the Sportsman's Groin

SPORT
Start date: December 3, 2014
Phase: N/A
Study type: Interventional

Sportsman's hernia is defined as a weakness or disruption of the posterior wall of the inguinal canal. Open hernia repair with or without mesh or laparoscopic techniques with mesh have been advocated in the treatment of sportsman's hernia and associated athletic pubalgia. The results of the operative treatment from single centers are reported to be good to excellent in between 70 - 90% of patients with the most promising results reported using an open minimal repair (OMR) technique. There are no randomized trials comparing open versus laparoscopic techniques regarding time for recovery and relief of pain. The aim of this randomized study is to compare the effectiveness of OMR technique in local or spinal anesthesia to endoscopic Total ExtraPeritoneal (TEP) technique in general anesthesia for the treatment of Sportsman´s hernia/athletic pubalgia. The primary endpoint is patient being free from intractable groin pain during sports activity or daily work four weeks after surgery.

NCT ID: NCT02292264 Completed - Ventral Hernia Clinical Trials

Risk Factors and Complications of Ventral Hernia Repair

Start date: September 2014
Phase:
Study type: Observational

The aim of this study is to evaluate risk factors and complications of ventral hernia repair. A retrospective study of journal files with patients undergoing ventral hernia repair, and an analyses of complications by use of the Clavien-Dindo classification of surgical complications.

NCT ID: NCT02272361 Completed - Cystocele Clinical Trials

Trial Comparing Laparoscopic Sacropexy and Vaginal Mesh Surgery for Women Cystocele Repair.

PROSPERE4
Start date: October 2014
Phase: N/A
Study type: Interventional

The primary objective of this study is to compare with PFDI-20 questionnaire the functional outcome of laparoscopic sacrocolpopexy and vaginal mesh surgery in the treatment of symptomatic exteriorised cystocele up to 4 years after surgery. The secondary objectives of this study are the following: 1. to compare the two techniques for anatomical results based on the clinical evaluation of patients with POP-Q. 2. to overall quality of life assessment and expectations of patients. 3. to compare the two techniques for the long-term safety. The evaluation will focus on the adverse effects of long-term sexual and genital symptoms, urinary and digestive functional symptoms, and chronic pelvic pain. 4. to compare the improvement of the functional outcome assessed by PFDI-20 questionnaire (matched-analysis before versus after).