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Inguinal Hernia clinical trials

View clinical trials related to Inguinal Hernia.

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NCT ID: NCT01521481 Completed - Inguinal Hernia Clinical Trials

Ultrasound-guided Inguinal Field Block (Genitofemoral, Iliohypogastric and Ilioinguinal Nerve Block) for Inguinal Hernia Surgery

U-IFB
Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the analgesic efficacy of an ultrasound-guided inguinal field block (block of the genitofemoral, iliohypogastric and ilioinguinal nerve).

NCT ID: NCT01505686 Completed - Pain Clinical Trials

MRI Findings in Inguinal Hernia

Start date: May 2012
Phase: N/A
Study type: Interventional

MRI imaging in clinically evident inguinal hernia is not routinely used. In other painful inguinal conditions (such as sportsmans hernia) inflammatory changes have been detected. The aim of the present study is to determine, whether similar inflammatory changes can be detected with MRI scan in inguinal hernia. Also, patient questionaires are used preoperatively and postoperatively to determine, if preoperative pain scores can be used as a predictive value for postoperative prolonged pain/neuralgia.

NCT ID: NCT01494272 Completed - Inguinal Hernia Clinical Trials

Analgesia in Children Using Caudal Epidural Ropivacaine

Start date: June 2012
Phase: N/A
Study type: Observational

Caudal epidural analgesia (caudal block)is used in standard pediatric anesthesia practice. It has been shown to be effective in managing postoperative pain in children undergoing abdominal and infraumbilical surgery (Tobias et al 1994). Furthermore, studies have shown that children receiving caudal blocks have secondary benefits such as lower narcotic and anesthetic requirements, more rapid awakening from general anesthesia, decreased time to discharge home, and fewer pain-related behaviors postoperatively (Conroy et al 1993, Tobias et al 1995, Tobias 1996). This proposed study involves the use of a caudal block in children undergoing elective inguinal herniorrhaphy or orchiopexy to evaluate the role of preemptive analgesia in pediatric pain management. We hypothesize that by inhibiting peripheral pain receptors with a caudal block before the onset of a painful stimulus, we can decrease central nervous system sensitization and reduce postoperative analgesic requirements

NCT ID: NCT01483313 Withdrawn - Inguinal Hernia Clinical Trials

Intelligence Changes Following Minor Surgery

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

Animal studies showed that many general anesthetics might result in neuron apoptosis and neurocognitive impairment in the developing brain. However results from human studies are conflicted. In present study, the investigators examined the association between early exposure to anesthesia and surgery for minor surgery and intelligence changes in adolescence using the Wechsler Intelligence Scale for Children.

NCT ID: NCT01467830 Withdrawn - Inguinal Hernia Clinical Trials

Open Inguinal Hernia Repair With Mesh,the Use of Absorbable Versus Non Absorbable Fixation Sutures

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

The purpose of this study is to determine the efficacy of mesh fixation using absorbable versus non-absorbable sutures.

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: 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: NCT01377181 Completed - Inguinal Hernia Clinical Trials

Laparoscopic Hernia Repair With Lateral Umbilicus Ligament for Children

Start date: January 2000
Phase: N/A
Study type: Observational

The role of laparoscopic surgery in pediatric inguinal hernia repair is clear. Laparoscopic hernia repair is especially advantageous for bilateral diseases and minimally invasive technique in children because it avoids vas injury. However, the problem of recurrent rate has not been resolved. The aim of this study was to refine the current criteria used the lateral umbilicus ligament covering the internal hernia opening region, and eliminated recurrence in laparoscopic inguinal hernia (LIH) repair in children. The investigators hypothesized that the lateral umbilicus ligament covering the internal hernia opening region after the laparoscopic purse-string knot would result in lower recurrence and the same operation relative complication

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: NCT01334775 Terminated - Inguinal Hernia Clinical Trials

Comparison of Self-adhering Mesh and Conventional Mesh in Inguinal Hernia Repair.

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

Inguinal hernia repair coincides with a high rate of postoperative pain, extending to over a year in 10-20% of patients. Although this is of major concern, early postoperative pain also has an important impact on patients and their ability to regain normal work and activities. Since inguinal hernia repair is the most frequently performed operation worldwide, a small reduction in loss of workdays can already have significant impact on financial issues. As for the origin of the pain, it might be the result of local inflammation caused by the mesh material, but also by nerve entrapment due to fixation techniques. The development of a new mesh which enables sutureless fixation, Cousin Biotech® Adhesix™, may overcome pain related to fixation techniques used in the open hernia repair procedure according to Lichtenstein. Furthermore, the Cousin Biotech® Adhesix™ mesh has already been in use in our institutions and surgeons familiarized themselves with the application. The investigators would like to conduct a multicentre randomised controlled clinical trial to compare the difference in early postoperative pain after unilateral primary inguinal hernia repair in males. The procedures will be performed in day surgery. Early postoperative pain is defined as the pain during the first month, with a special interest in the first two weeks. In addition, the investigators want to measure the possible benefit in terms of time to return to work, daily activities, quality of life, operation length, complications and long term postoperative pain.