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Hernia clinical trials

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NCT ID: NCT01578538 Recruiting - Hernia Clinical Trials

Safety of Mesh Used Repairs in Emergency Abdominal Wall Hernias. Prospective Randomized Multicenter Trial

hernia
Start date: February 2012
Phase: N/A
Study type: Interventional

Repairing of emergency (strangulated) abdominal wall hernias with mesh may cause infective complications.

NCT ID: NCT01501682 Recruiting - Ventral Hernia Clinical Trials

Long Term Complaints After Elective Repair for Small Umbilical or Epigastric Hernias

Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to compare the long-term complaints after ventral hernia repair after insertion of different types of mesh compared with primary suture. Also recurrence of hernia will be discussed.

NCT ID: NCT01450345 Recruiting - Postoperative Pain Clinical Trials

Efficacy of Pre-operative Oral Pregabalin in Ambulatory Inguinal Hernia Repair for Post Operative Pain

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The study carry out is to determine whether the use of oral pregabalin premedication to assess the analgesic efficacy, opiod sparing, adverse effect and clinical value in post-operative pain management.

NCT ID: NCT01421550 Recruiting - Liver Cirrhosis Clinical Trials

Conservative Treatment Versus Elective Repair of Umbilical Hernia in Patients With Ascites and Liver Cirrhosis

CRUCIAL
Start date: January 2011
Phase: Phase 3
Study type: Interventional

The purpose of the present study is to investigate whether or not to perform elective surgical repair of umbilical hernias in patients with liver cirrhosis and ascites. There are no other randomized controlled trials in this area. The optimal management in patients with umbilical hernias and liver cirrhosis with ascites is not clear yet. The general surgical opinion is that umbilical hernias in patients with ascites should not be corrected because of the supposedly high operative risks and high recurrence rates. Conservative treatment, however, can have severe complications resulting in emergency repair. Such operations carry a higher risk of complications than elective operations, particularly in this group of patients. Prospective and retrospective series showed us that elective hernia repair in this specific patient group is safe without major complications or high recurrence rates. The aim of this study is to asses the optimal timing of correction of umbilical hernia in patients with liver cirrhosis and ascites.

NCT ID: NCT01398215 Recruiting - Ventral Hernia Clinical Trials

Natural Orifice Translumenal Endoscopic Surgery (NOTES): Laparoscopic Assisted Transvaginal Ventral Hernia Repair

NOTES
Start date: January 2009
Phase:
Study type: Observational

This is a prospective chart review/data collection study of natural orifice translumenal endoscopic surgery (NOTES) for ventral hernia repair, that will include questionnaires administered throughout the study. Subjects enrolled will be those intending to have a transvaginal NOTES ventral hernia repair. Data will be collected and reviewed through 12 months post-op.

NCT ID: NCT01391455 Recruiting - Inguinal Hernia Clinical Trials

Isolation of the Spermatic Cord in Mesh Inguinal Hernia Repair

Start date: July 2011
Phase: N/A
Study type: Interventional

There are in excess of 1 million operations performed annually to repair inguinal hernias, mostly in the male population. Unfortunately, some patients continue to suffer both groin or testicular pain for varying lengths of time postoperatively. This can lead to a severe degradation of the patient's lifestyle, work habits and sexual function. The origin of the pain is felt to be secondary to the inflammatory reaction caused by the mesh. This also involves the spermatic cord and its structures, leading to orchidinia and possibly azospermia.

NCT ID: NCT01363830 Recruiting - Clinical trials for Lumbar Disc Herniation

Short Versus Long Post-Operative Restrictions Following Lumbar Discectomy

Start date: August 2009
Phase: N/A
Study type: Interventional

Post-operative restrictions following lumbar discectomy is a controversial topic. While the most widely accepted protocol restricts bending, lifting, and twisting for four to six weeks following discectomy, a number of studies support an early return to full activity without restriction. Since the goal of discectomy is to promptly provide pain relief and a return to a fully active lifestyle, perhaps post-operative restrictions are more hindering than beneficial. Hypothesis: Post-operative restrictions following lumbar discectomy do not influence reherniation rate. Specific Aim 1: To compare the reherniation rates between the 6-weeks of restriction and the 2-weeks of restriction groups. Specific Aim 2: To determine the return to full activity and return to work dates of both the 6-weeks of restriction and 2-weeks of restriction groups. Specific Aim 3: To assess the health outcomes of both the 6-weeks of restriction and 2-weeks of restriction groups.

NCT ID: NCT01348477 Recruiting - Inguinal Hernia Clinical Trials

Comparison Between Elliptical Domed Mesh Technique and Lichtenstein Technique in Inguinal Hernia

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

The investigators describe a new surgical technique for inguinal hernia open repair, which will be compared with the Lichtenstein technique. The investigators seek to find the difference between the two techniques in postoperative pain.

NCT ID: NCT01326039 Recruiting - Inguinal Hernia Clinical Trials

Ultrasound-guided Ilioinguinal-iliohypogastric Block for Inguinal Hernia Repair

Start date: May 2010
Phase: Phase 4
Study type: Interventional

Aim: To investigate whether ultrasound-guided perineural administration of 20 ml bupivacaine 5 mg/ml vs 20 ml isotonic saline at the ilioinguinal-iliohypogastric nerves have a clinically analgesic effect after unilateral open inguinal hernia repair.

NCT ID: NCT01136603 Recruiting - Hernia Clinical Trials

TIGR vs Polypropylene (Permanent) Mesh: Randomised Trial

Start date: July 2010
Phase: Phase 2
Study type: Interventional

Hypothesis: TIGR mesh as a reconstruction material is a more effective mesh for the repair of the abdominal wall post lipectomy, transverse rectus abdominis myocutaneous (TRAM) / deep inferior epigastric perforator (DIEP) flap.