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Abdominal Wall Hernia clinical trials

View clinical trials related to Abdominal Wall Hernia.

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NCT ID: NCT03765060 Recruiting - Clinical trials for Abdominal Wall Defect

The Efficacy and Security of the Small Stitch Technique in Emergency Surgery

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

This study evaluates the abdominal closure technique in emergency surgery. Half of participants will be perform the classic Large Stitch technique, while the other half will undergo the Small Stitch technique.

NCT ID: NCT03643718 Not yet recruiting - Acute Pancreatitis Clinical Trials

WSES International Register of Emergency Surgery

Start date: September 2018
Study type: Observational [Patient Registry]

The WIRES project (WSES International Registry of Emergency General Surgery) has been set up to allow to all the EGS (Emergency General Surgery) surgeons to register their activity and to obtain a worldwide register of surgical emergencies. This will give the opportunity to evaluate results on a macro-data basis and to give index allowing stratifying, evaluating and improving the outcomes.

NCT ID: NCT03310905 Not yet recruiting - Clinical trials for Transplant;Failure,Kidney

Abdominal Wall Transplant

Start date: May 1, 2018
Phase: Phase 2
Study type: Interventional

The purpose of this protocol is to determine the safety and efficacy of abdominal wall transplantation as a treatment for the reconstruction of abdominal wall defects. Abdominal wall transplantation may be performed alone or in combination with another transplant.

NCT ID: NCT03198871 Recruiting - Pancreatic Diseases Clinical Trials

IV Acetaminophen for Post-Operative Pain Management in Enhanced Recovery After Surgery (ERAS) Population

Start date: May 24, 2018
Phase: Phase 4
Study type: Interventional

Number of patients with unsatisfactory pain relief defined as average visual analog scale (VAS) more than 5 with or without requirement of IVPCA for pain relief during the first 48 hours postoperative period will be compared between the two groups and form the primary outcome for the study. Postoperative pain intensity will be measured by Visual Analog Scale (VAS) with 0- being no pain and 10-being maximum pain and the analgesic efficacy in both groups will also be evaluated by the amount of total narcotic consumption (measured with IV morphine equivalent doses of analgesics used to provide pain relief).

NCT ID: NCT00908193 Completed - Clinical trials for Abdominal Wall Hernia

Laparoscopic "DA VINCI" Robot Assisted Abdominal Wall Hernia Repair

Start date: July 2007
Phase: Phase 4
Study type: Interventional

The aim of this study is to prove the superiority of the robotic assistance in laparoscopic repair of abdominal wall hernias . In this monocentric randomized controlled trial, the use of the DA VINCI robot might reduce the post-operative pain of the patient resulting in a 40% reduction of morphine consumption.