Clinical Trials Logo

Hernia, Inguinal clinical trials

View clinical trials related to Hernia, Inguinal.

Filter by:

NCT ID: NCT04850131 Completed - Postoperative Pain Clinical Trials

Desarda Repair Compared to Lichtenstein Repair for the Treatment of Inguinal Hernias

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

The Lichtenstein technique for hernia repair is safe and simple, but the underlying mesh prosthesis has its setbacks, as it acts as a mechanical barrier5. The mesh does not provide mobile and the physiologically dynamic posterior wall. The most dangerous complication associated with the mesh prosthesis is its migration from the abdominal cavity's primary implantation site. The relatively knew technique developed by Dr. Desarda does not utilize the synthetic mesh rather it uses a strip of external oblique aponeurosis to strengthen the posterior wall. Our study has compared the two methods regarding various aspects.

NCT ID: NCT04839848 Completed - Chronic Pain Clinical Trials

Chronic Postoperative Pain After the Lichtenstein Groin Hernioplasty

Start date: September 1, 2012
Phase:
Study type: Observational [Patient Registry]

The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) after Lichtenstein repair of groin hernia, depending on mesh type and fixation suture material. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

NCT ID: NCT04838028 Completed - Chronic Pain Clinical Trials

Chronic Postoperative Pain After Laparoscopic Groin Hernia Repair

Start date: September 1, 2012
Phase:
Study type: Observational

The study attempts to quantify the relative risks for chronic postoperative inguinal pain (CPIP) depending on different combinations of mesh and mesh fixation. For this purpose the investigators will analyze data from the Swedish Hernia Registry (SHR).

NCT ID: NCT04815707 Recruiting - Inguinal Hernia Clinical Trials

Treatment of Occult Inguinal Hernias

Start date: October 22, 2021
Phase: Phase 2
Study type: Interventional

Inguinal hernias are a common surgical problem. Best management of occult inguinal hernias, defined as hernias unable to be felt on physical exam, is unknown. From prior studies we know that most inguinal hernias will eventually become symptomatic and require surgery (70%). However, doing a repair on a very small, occult hernia may open the patient up to surgical complications, like chronic pain, earlier than necessary. This will be a multi-center randomized controlled trial of surgical repair versus expectant management of occult inguinal hernias. Patients undergoing laparoscopic unilateral inguinal hernia repair will be included. At the time of surgery, the surgeon will determine if there is an occult hernia contralateral side. If present, patients will be randomized to repair of the occult side or expectant management of the occult side. After 1 year post-operative data has been assessed, a decision tool will be created and administered to patients to aid in their decision making about treatments for their hernia.

NCT ID: NCT04806828 Completed - Inguinal Hernia Clinical Trials

Preoperative Score of Inguinal Hernias. Is it Useful to Predict Outcomes

POINTHER
Start date: January 1, 2019
Phase:
Study type: Observational [Patient Registry]

To analyze and validate a preoperative score of difficulty of inguinal hernias and its correlation with postoperative outcomes

NCT ID: NCT04805580 Not yet recruiting - Clinical trials for Inguinal Hernia,Quadratus Lumborum Block , Unilateral Intrathecal Block

Qudratus Lumborum Block Versus Unilateral Intrathecal Block for Inguinal Hernia Repair

Start date: May 2021
Phase: N/A
Study type: Interventional

compare between Quadratus lumborum block and unilateral intrathecal block for patients undergoing inguinal hernia repair regarding the quality of anesthesia and hemodynamic stability of patients.

NCT ID: NCT04792164 Not yet recruiting - Inguinal Hernia Clinical Trials

Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

A hernia occurs when an organ 'like intestines' or fatty tissue protrude through a weak point in muscle or connective tissue and one of the most common types of hernia is inguinal. Inguinal hernia defined as a bulge in the inguinal region or scrotum, may be accompanied by dull or burning pain, which worsens by exercise or cough. There are 2 types of inguinal hernia: direct and indirect. Direct inguinal hernia occurs because of a defect or weakness in the transversalis fascia area of the Hesselbach triangle. On the other hand, the indirect inguinal hernia which is the most common inguinal hernia follows the tract of inguinal canal and result from a persistent processus vaginalis. Immediate pain after inguinal herniorrhaphy delays the ambulation which leads to delay in the hospital discharge. Besides that, is the chronic pain that affect 50% of patients which is an important issue that needs to be dealt with. Our aim of this study, is to compare between postoperative period in the patients who received US guided nerve block and in patients who received infiltration only before open inguinal hernia repair, and to show that pre-emptive local anaesthesia will result in better pain control, less postoperative complication, earlier mobilisation, earlier recovery and less analgesia consumption by patients.

NCT ID: NCT04785430 Enrolling by invitation - Inguinal Hernia Clinical Trials

Incarceration Risk Factors in Inguinal Hernia.

Start date: January 1, 2021
Phase:
Study type: Observational [Patient Registry]

It is known that strangulation or necrosis of the intestine within the hernia sac of inguinal hernia increases mortality and morbidity in patients. However, the risks of incarceration in hernias have not been fully revealed.To better understand the factors associated with incarceration in inguinal hernia, the investigators will examine patients who will apply to our clinic for inguinal hernia and undergo elective and emergency inguinal hernia surgery.

NCT ID: NCT04779918 Recruiting - Hernia, Inguinal Clinical Trials

Ventral or Inguinal Hernia, Robotically Repaired With OviTex Mesh

BRAVOII
Start date: April 14, 2021
Phase: N/A
Study type: Interventional

This study is designed to evaluate the post-operative complications and hernia recurrence following the use of OviTex in subjects with ventral or inguinal hernias. Up to 160 subjects will participate in the study from up to 20 investigator sites.

NCT ID: NCT04764760 Completed - Inguinal Hernia Clinical Trials

Biomechanically Compatible,Minimally Invasive Technique for Recurrence Free Groin Hernia Repair

Start date: January 1987
Phase: N/A
Study type: Interventional

"A bio-mechanically compatible, minimally invasive technique for recurrence-free groin hernia repair by implantation of Tensiflex mesh prosthesis for the enhancement of the tissue tensile strength of the fascia transversalis."