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Hernia clinical trials

View clinical trials related to Hernia.

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NCT ID: NCT04808063 Recruiting - Clinical trials for Incisional Hernia of Midline of Abdomen

Algorithm for Prophylactic Mesh Use in Emergency Laparotomy.

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

Use of informed algorithm for patients selection of prophylactic mesh aplication after midline laparotomy in emergency surgery.

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: NCT04801394 Completed - Incisional Hernia Clinical Trials

Retrospective Analysis on Large Incisional Hernia in High Risk Patients

Start date: April 1, 2010
Phase: N/A
Study type: Interventional

Large incisional hernia (LIH) is a challenging condition where the abdominal wall is hopelessly compromised. Nowadays the best treatment option in this particularly frail subset of patients is a major issue. The Auhtors proposed the clinical experience with an innovative approach with the composite Free Lateral Polypropylene prosthesis (FLaPp®) mesh fashioned as "neoperitoneum" analyzing its feasibility and short/medium term results.

NCT ID: NCT04795934 Recruiting - GERD Clinical Trials

Multicenter Single-Blind RCT of CTIF Versus LNF For Treatment of GERD in Patients Requiring Hiatal Hernia Repair

CTIF
Start date: January 26, 2021
Phase: N/A
Study type: Interventional

This single-blind randomized control study will follow 142 subjects across 7 sites randomized on a 1:1 ratio to compare treatment efficacy and safety between TIF and LNF in GERD patients with hiatal hernia undergoing hernia repair.

NCT ID: NCT04794582 Recruiting - Clinical trials for Postoperative Complications

Prevention of Incisional Hernia After Renal Transplantation

Start date: August 31, 2022
Phase: N/A
Study type: Interventional

Randomized clinical trial to determine the efficacy of mesh reinforcement in laparotomy closure in renal transplantation as measured by reduction in the incidence of incisional hernia at 2 years post-transplantation.

NCT ID: NCT04793009 Completed - Hernia Clinical Trials

Prophylactic Funnel Mesh to Prevent Parastomal Hernia in Permanent End Colostomy After Abdomino-perineal Resection

Start date: January 1, 2013
Phase:
Study type: Observational

This retrospective study asses if a prophylactic, funnel-shaped, intraperitoneal mesh prevents parastomal hernia in patients undergoing abdominoperineal rectum resection with permanent end colostomy.

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: NCT04788771 Completed - Pain Score Clinical Trials

Comparison of Tracheal Intubation vs Laryngeal Mask Airway in Laparoscopic Total Extraperitoneal Hernia Repair

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Patient comfort and satisfaction of inguinal hernia repairs can be affected by the anesthesia technique chosen in addition to the surgical method. In our study, we aimed to compare the anesthesia method used in patients during laparoscopic total extraperitoneal hernia repair, which is a minimally invasive method.It was planned to evaluate the patients' quality of life, pain conditions, additional medical support needs for pain, length of hospital stay, duration of surgery, complications during and after surgery and recurrence rates.In addition, it was planned to compare the effects of the anesthesia method used on the lung capacity of the patients. The most important achievement of the study will be to show that laparoscopic hernia repair, which is frequently performed by intubation, can be performed safely with the Laryngeal mask.

NCT ID: NCT04788199 Completed - Bariatric Surgery Clinical Trials

Novel Technique in Closure of Mesenteric Defects After Laparoscopic Roux-en-Y Gastric Bypass and Its Effect on Internal Hernia: a Case-control Study

Start date: June 15, 2018
Phase:
Study type: Observational

This study is to investigate the rate of internal hernia after laparoscopic Rox-en-Y gastric bypass when the defects are closed using cyano-acrylate glue.