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Laparotomy clinical trials

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NCT ID: NCT01723280 Completed - Laparotomy Clinical Trials

Supplemental Oxygen - Effect on Occurrence of Subsequent Cancer After Abdominal Surgery (Follow-up of the PROXI Trial)

PROXI
Start date: October 2006
Phase: N/A
Study type: Observational

Aim: to investigate the effect of a high inspiratory oxygen fraction (FiO2) given during and after laparotomy procedures on occurrence of a subsequent, new or recurrent, cancer diagnosis at a long-term follow-up. Background: A high inspiratory oxygen fraction (FiO2 = 0.80) has been linked to prevention of surgical site infection, but the Danish randomized clinical multicenter trial, the PROXI trial, found no difference in frequency of surgical site infection. In fact, long-term mortality was significantly increased with a hazards ratio of 1.30 in patients receiving 80% oxygen, and this appeared to be statistically significant in patients undergoing cancer surgery, but not in non-cancer patients. At this point, no convincing mechanism explains the observed increased mortality after hyperoxia, as the long-term pathophysiological effects of oxygen are not fully understood. Primary hypothesis of this follow-up study of the PROXI trial: Use of 80% oxygen increase the frequency of patients with a subsequent, new or recurrent, cancer.

NCT ID: NCT01719796 Recruiting - Laparotomy Clinical Trials

Effect of TAP Block on Ventilatory Function Following Abdominal Surgery

KTAP
Start date: October 2012
Phase: Phase 2
Study type: Interventional

Abdominal surgery impairs ventilation. Postoperative pain accounts for this impairment. Regional analgesia is known to reduce pain, thus to limit ventilatory impairment. The investigators hypothesized bilateral continuous transverse abdominal plan block would reduce ventilatory impairment following abdominal surgery.

NCT ID: NCT01201655 Recruiting - Liver Cirrhosis Clinical Trials

Study of the Impact of Hypersplenism and Splenectomy on Hepatocarcinogenesis in Patients With Posthepatitic Cirrhosis

Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the impact of splenectomy coupled with portal-azygous disconnection on hepatocarcinogenesis in patients with post-hepatitic cirrhosis after hepatitis B or C virus infection by retrospective case-control study,We hope to find a new idear and method to prevent or cure HCC.

NCT ID: NCT01098175 Not yet recruiting - Thoracotomy Clinical Trials

Peritoneal Cavity Conditioning During Open Surgery.

Start date: April 2010
Phase: N/A
Study type: Observational

Given the observations in animal models and the available data in the human our hypothesis is that peritoneal cavity conditioning (carbon dioxide with 4% of oxygen and 10% of N2O, 100% humidification at 32°C,) during open surgery, will result in an important decrease in postoperative peritoneal inflammation, postoperative pain, and will restore bowel transit faster.

NCT ID: NCT01040013 Completed - Laparoscopy Clinical Trials

Gut Oxygenation and Laparoscopy

Start date: March 2008
Phase: Phase 2
Study type: Interventional

Patients with left-colon cancer will be randomized to laparoscopic or laparotomic operation. during surgery and for 6 days after operation, intestinal oxygen tension and ischemia-reperfusion injury markers will be evaluated to understand if pneumoperitoneum is associated with reduced splanchnic blood flow and ischemia-reperfusion injury.

NCT ID: NCT00972920 Completed - Laparotomy Clinical Trials

TAP Block for Gynaecological Laparotomies - a Comparison of Ultrasound-guided Block and Blind Technique

Start date: August 2009
Phase: N/A
Study type: Interventional

Transversus abdominis plane (TAP) block is an application of local anaesthetic solution into the plane between internal oblique and transversus abdominis muscles at the triangle of Petit located superiorly to the iliac crests bilaterally. Anterior divisions of segmental spinal nerves, which provide innervation to the abdominal wall, run inside this compartment. TAP block been shown to provide good postoperative pain relief following surgical laparotomies, gynaecological laparotomies, appendicectomies, inguinal hernia repairs and open prostatectomies. The goal of this study is to compare the effect of blind and ultrasound-guided TAP block on postoperative pain relief and morphine consumption following to gynaecological laparotomies. Null research hypothesis for the study is that there is no difference between the performance (as defined by morphine consumption and patient satisfaction/ pain scores) of the TAP block procedure via 'blind' or ultrasound guided techniques for gynaecological laparotomies.

NCT ID: NCT00645684 Completed - Clinical trials for Gastrointestinal Diseases

Clinical Use of an Absorbable Coated Suture Material in Surgery (Safil)

Start date: April 1998
Phase: Phase 4
Study type: Interventional

The purpose is to test a coated polyglycolic acid multifilament suture in gastrointestinal surgery as part of a controlled randomized single blinded parallel group trial. The applicability and safety of the strand material used in two suture techniques (2-layer suture technique vs. 1-layer running) are to be tested on the basis of handling characteristics, the operative time consumed for the construction of the 1st anastomosis, the average time of the hospital duration for both patient groups, and the frequency of postoperative complications after discharge, 1 month and a maximum of 3-4 months. The used suture units are counted and the length of sutures determined which will be an indirect measurement of the costs of suture material for the two techniques.

NCT ID: NCT00637936 Completed - Laparotomy Clinical Trials

Respiratory Effects of Perioperative Oxygen During General Anaesthesia

Start date: March 2008
Phase: Phase 4
Study type: Interventional

Aim: To investigate the effect of high intra- and postoperative oxygen concentration (80%, as opposed to normally 30%) on pulmonary gas exchange and other pulmonary complications after abdominal surgery. Background: Previous studies have shown possible beneficial effects of high perioperative oxygen concentration on surgical wound infection and healing, but all pulmonary effects are not clarified. Change in perioperative PaO2/FiO2 and shunt-fraction, measured by a gas rebreathing technique, can describe pulmonary oxygenation. This could add knowledge to the pulmonary effects of high vs. normal oxygen concentration. Primary hypothesis of study: Perioperative use of a 80% oxygen concentration reduces the PaO2/FiO2-index compared to 30% oxygen.

NCT ID: NCT00544583 Recruiting - Hernia Clinical Trials

Continuous Versus Interrupted Abdominal Wall Closure After Emergency Midline Laparotomy

CONTINT
Start date: November 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Patients undergoing primary midline laparotomy for an emergency surgical intervention with a suspected septic focus in the abdominal cavity.

NCT ID: NCT00514566 Terminated - Laparotomy Clinical Trials

PDS vs Polyamide for Midline Abdominal Closure

PPMAC
Start date: October 2004
Phase: N/A
Study type: Interventional

Within the last decade the customary trend of using non absorbable sutures has changed, with numerous studies and meta-analyses advocating the use of slowly absorbable sutures, claiming comparable wound strength with significantly lower incidence of wound complications. It was the objective of this randomized clinical trial to compare two universally accepted suture materials, the non-absorbable Nylon and the slowly absorbable Polydioxanone for midline abdominal closure in the Indian context.