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Inguinal Hernia clinical trials

View clinical trials related to Inguinal Hernia.

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NCT ID: NCT05706662 Completed - Inguinal Hernia Clinical Trials

Dynamic Scaffold Versus Lichtenstein Open Hernioplasty.

DYSLOH
Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Evaluating the outcomes of patients undergoing open anterior inguinal hernioplasty comparing two different techniques: Lichtenstein/plug and mesh and ProFlor. The outcomes of these two groups of patients, respectively the Lichtenstein inguinal hernia repair with static flat mesh and the defect obliteration with 3D dynamic scaffold Proflor, are compared in respect to defined variables along stages: intraoperative, early and long term postoperative.

NCT ID: NCT05702710 Completed - Surgery Clinical Trials

Minimal Invasive Treatment of Inguinal Hernia in Neonates

Start date: January 30, 2023
Phase:
Study type: Observational

In this study, preoperative physical examination findings, peroperative findings and data, and postoperative follow-up results of newborns who underwent inguinal hernia repair with PIRS ("Percutaneous Internal Ring Suturing") method will be evaluated retrospectively.

NCT ID: NCT05681338 Completed - Inguinal Hernia Clinical Trials

Effect of the Coughing Technique During Subcutaneous Heparin Injection

Start date: March 17, 2022
Phase: N/A
Study type: Interventional

Objective: to examine the effect of the medium intensity coughing technique during subcutaneous low molecular weight heparin injection on pain severity and individual satisfaction in general surgery patients. Method: a prospective, quasi-experimental study included 100 patients who had prescribed a subcutaneous low molecular weight heparin injection once in 24 hours. Each patient received two injections by the same researcher using standard injection technique with medium intensity coughing technique and only standard injection technique.

NCT ID: NCT05672680 Completed - Inguinal Hernia Clinical Trials

Transabdominal Plane (TAP) Blocks for Inguinal Hernia Repairs

Start date: December 9, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this double-blind clinical trial is to examine outcomes and pain control after surgery in patients who underwent laparoscopic inguinal hernia repair (IHR) with the use of perioperative transabdominal plane (TAP) block. Research Question: Does transabdominal plane block improve pain when undergoing inguinal hernia repair? The endpoints include whether preoperative TAP blocks improve pain score (primary end point) and decrease opioid use (secondary endpoint) after an inguinal hernia repair. Other end points- complications after surgery.

NCT ID: NCT05610943 Completed - Post Operative Pain Clinical Trials

Comparison of The Quadratus Lumborum Block and Ilioinguinal Iliohypogastric Nerve Block

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

Perioperative and postoperative pain control in pediatric patients is a frequently neglected issue. Regional anesthesia applications reduce adverse drug events by minimizing opioid consumption and provide effective and safe analgesia. In recent years, quadratus lumborum block has emerged as an alternative regional anesthesia technique and it has been shown to provide analgesia as effectively as caudal block in children, and in a limited number of studies it has been said that it is more effective than transversus abdominis plane block. There are few studies in the literature comparing ilioinguinal iliohypogastic nerve block and quadratus lumborum block in children.

NCT ID: NCT05549492 Completed - Pain, Postoperative Clinical Trials

Transversus Abdominis Plane Block With or Without Buprenorphine After Inguinal Hernia Surgery

Start date: January 1, 2021
Phase: Phase 1
Study type: Interventional

Buprenorphine intravenous, sublingual, and transdermal patches have been researched for their antihyperalgesic effects, although peripherally mediated effects have not been examined in Egypt surprisingly

NCT ID: NCT05476510 Completed - Inguinal Hernia Clinical Trials

M-Tapa vs OSTAP for Laparoscopic Inguinal Hernia Repair Surgery

Start date: August 10, 2022
Phase: N/A
Study type: Interventional

Inguinal hernia repair is the most common of abdominal surgical procedures and is usually performed laparoscopically. Many factors play a role in the pain that develops after surgery and is generally considered to be visceral pain. Phrenic nerve irritation due to CO2 insufflation into the peritoneal cavity, abdominal distention, tissue trauma, sociocultural status, and individual factors are the factors that play a role in the occurrence of this pain. Modified Perichondral Approach Thoracoabdominal Nerve (M-TAPA) block performed with ultrasound (US) is a new block that provides effective analgesia in the anterior and lateral thoracoabdominal areas, where local anesthetic is applied only to the lower side of the perichondral surface. M-TAPA block is a good alternative for analgesia of the upper dermatome levels and abdominal lateral wall and may be an opioid-sparing strategy with satisfactory quality recovery in patients undergoing laparoscopic surgery. Oblique Subcostal Transversus Abdominis Plane Block (OSTAP) is one of the body blocks used especially for postoperative analgesia. OSTAP, defined by Hebbard in 2010, is a subcostal version of the Transversus abdominis plane block (TAP block), based on the injection of local anesthetic from the lower edge of the costal margin, obliquely between the obliquus externus and Transversus abdominis muscles. This study aimed to compare the efficacy of US-guided M-TAPA block and OSTAP block for postoperative analgesia management after laparoscopic inguinal hernia repair surgery. Our primary aim is to compare postoperative pain scores (0. hour NRS), and our secondary aim is to evaluate the use of rescue analgesics (opioids), side effects associated with opioid use (allergic reaction, nausea, vomiting), and patient satisfaction (Likert scale).

NCT ID: NCT05379374 Completed - Inguinal Hernia Clinical Trials

Effects of Morphine Added to Bupivacaine in Transversus Abdominis Plane Block for Inguinal Hernia Repair

Start date: August 18, 2018
Phase: N/A
Study type: Interventional

This study is conducted to determine whether morphine added to bupivacaine in ultrasound guided (USG) transversus abdominis plane (TAP) block has beneficial effects than bupivacaine alone in providing postoperative analgesia for inguinal hernia surgery.

NCT ID: NCT05172908 Completed - Inguinal Hernia Clinical Trials

The Effect of Dexamethasone on Rebound Pain in Patients Receiving Ilioinguinal and Iliohypogastric Nerve Block

Start date: January 6, 2022
Phase: N/A
Study type: Interventional

Rebound pain is a newly defined phenomenon, observed within the first 24 hours after the operation. Open inguinal hernia repair is a common surgical procedure that can be associated with pain of the either acute or chronic character. A peripheral nerve block of the ilioinguinal (IIN) and iliohypogastric (IHN) nerves is a relatively well-known method for postoperative pain management. However, rebound pain after IIN/IHN block resolution may reduce its overall benefit. The primary aim is to assess whether intravenous dexamethasone reduces postoperative opioid consumption and the incidence of rebound pain in patients undergoing unilateral hernia repair in adults.

NCT ID: NCT05159232 Completed - Inguinal Hernia Clinical Trials

Length of Hospital Stay in Laparoscopic Transabdominal Preperitoneal Vs. Open Mesh Repair in Inguinal Hernia: A Randomised Controlled Trial

Start date: September 1, 2018
Phase: N/A
Study type: Interventional

To compare the mean length of hospital stay in laparoscopic trans abdominal preperitoneal repair versus open mesh repair in patients undergoing inguinal hernia repair with mesh.