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Inguinal Hernia Repair clinical trials

View clinical trials related to Inguinal Hernia Repair.

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NCT ID: NCT06389318 Completed - Clinical trials for Inguinal Hernia Repair

Buccal Midazolam Versus Intranasal Dexmedetomidine Plus Oral Chloral Hydrate in Inguinal Hernia Repair

Start date: March 26, 2023
Phase: N/A
Study type: Interventional

Inguinal hernia surgery is one of the most common surgical procedures in early infancy. Preoperative anxiety remains a vexing issue, and it exists in nearly 50% of pediatric patients

NCT ID: NCT06098105 Completed - Ultrasound Clinical Trials

Laparoscopic vs Ultrasound-Guided Transversus Abdominis Plane Block vs Laparoscopic Intraperitoneal Instillation of Local Anesthetic in Pediatrics

Start date: October 24, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to compare laparoscopic -assisted, ultrasound-guided transversus abdominis plane block and laparoscopic intraperitoneal instillation of local anesthetic in pediatrics undergoing inguinal hernia repair.

NCT ID: NCT05873582 Completed - Clinical trials for Inguinal Hernia Repair

Robotic Minimally Invasive Inguinal Hernia Repair With Dexter

RAS-Ahead
Start date: June 2, 2023
Phase:
Study type: Observational

This study aims to confirm the perioperative and early postoperative safety and clinical performance (efficacy) of the Dexter Robotic System, in patients undergoing primary transperitoneal unilateral or bilateral inguinal hernia repair.

NCT ID: NCT05559437 Completed - Pain, Postoperative Clinical Trials

Ultrasound-guided Ilioinguinal/Iliohypogastric Nerve Block

Start date: October 1, 2022
Phase: Phase 1
Study type: Interventional

Abdominal wall hernias are common, with a prevalence of 1.7% for all ages and 4% for those aged over 45 years. Inguinal hernias account for 75% of abdominal wall hernias, with a lifetime risk of 27% in men and 3% in women. Repair of inguinal hernia is one of the most common operations in general surgery

NCT ID: NCT05073055 Completed - Postoperative Pain Clinical Trials

Spinal Anesthesia Versus Erector Spina Plane Block

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

The primary aim of our study was to use spinal anesthesia for unilateral inguinal hernia surgery and lumbar erector spina block supported by local infiltration anesthesia in terms of operation time, intraoperative hemodynamic data, motor block onset time, block termination time, analgesic need, discharge time, patient satisfaction, surgeon satisfaction. is to compare. Its second purpose is to observe nausea, vomiting, urinary retention, headache, chills, bleeding, wound infection.

NCT ID: NCT03678272 Completed - Inguinal Hernia Clinical Trials

Comparative Study of Inguinodynia After Inguinal Hernia Repair

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

To evaluate the postoperative pain and the relapse after the repair of the inguinal hernia by Lichtenstein technique with four different mesh types with different types of fixation in patients undergoing major ambulatory surgery.

NCT ID: NCT03033381 Completed - Clinical trials for Inguinal Hernia Repair

A Comparison of Testicular Volume and Blood Flow in Patients With Inguinal Hernia, Hydrocele, and Cord Cyst

IHR
Start date: April 2016
Phase: N/A
Study type: Interventional

Here, investigators aimed to evaluate the effect of inguinal operations performed with a modified Ferguson technique upon testicular volume and blood flow. This study involved 23 patients receiving surgery for inguinal hernia, hydrocele, and cord cyst. The color Doppler ultrasound (CDUS) was used to assess testicular volume and blood flow before and after a modified Ferguson technique surgery. The pre- and postoperative testicular volume and blood flow were compared with the contralateral testes. Statistical Package for the Social Sciences (SPSS) software was used to statistically analyze the data arising; the Mann-Whitney U test and Friedman test were used to compare samples, and P < 0.05 was accepted as statistically significant.

NCT ID: NCT02537860 Completed - Clinical trials for Inguinal Hernia Repair

Paravertebral Block for Inguinal Hernia Repair in Elderly

Start date: December 2015
Phase: N/A
Study type: Interventional

This prospective double-blinded clinical trial is intended to compare three nerve stimulator- guided paravertebral block injections versus five injections for elderly patients undergoing hernia repair regarding intraoperative hemodynamic stability and postoperative pain.

NCT ID: NCT02500056 Completed - Clinical trials for Inguinal Hernia Repair

Single-centre Single-blinded Randomised Study Evaluating the Impact of Mesh Pore Size on Chronic Pain After Lichtenstein Hernioplasty

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

The aim of the present study is to determine whether usage of mesh with larger pores, compared with mesh with smaller pores, would result in decreased rate of chronic pain after open inguinal hernia repair. The patients are randomized into two study gropus receiving mesh with different pore size. Clinical follow-up examination will be performed 1 week, 1 month, 6 months and 3 years after the operation.