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Intestinal Obstruction clinical trials

View clinical trials related to Intestinal Obstruction.

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NCT ID: NCT01899885 Completed - Clinical trials for Intestinal Obstruction

Acute High-risk Abdominal Surgery Study - an Optimized Perioperative Course

AHA
Start date: June 2013
Phase: N/A
Study type: Interventional

The objective of this study is to implement an optimized perioperative course for patients undergoing acute high-risk abdominal surgery in order to improve the outcome. The optimized perioperative course consists of a number of interventions carried out before, during and after surgery.

NCT ID: NCT01834430 Completed - Clinical trials for Inflammatory Intestinal Obstruction

Effects of Delayed Enteral Nutrition on Inflammatory Responses and Immune Function Competence in Critically Ill Patients With Prolonged Fasting

Start date: February 2010
Phase: Phase 3
Study type: Interventional

Different studies suggest that early enteral nutrition (EEN) has benefits in reducing infectious complications, there is no data that addresses whether delayed enteral nutrition (EN) is detrimental and if it may have effects on inflammatory responses and immune function.

NCT ID: NCT01596777 Completed - Clinical trials for Intestinal Obstruction

Effects of 500 mg Immediate Release and Extended Release Methylnaltrexone on Loperamide-induced Delay of the Oro-cecal and Whole-gut Transit Time in Healthy Subjects

LOP-MNTX-2009
Start date: January 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to describe the effects of methylnaltrexone in preventing loperamide-induced delay of the oro-cecal and whole-gut transit time and measure pharmacokinetics of methylnaltrexone after subcutaneous and oral administration of immediate release and extended release capsules.

NCT ID: NCT01596764 Completed - Clinical trials for Intestinal Obstruction

Effects of Methylnaltrexone in Comparison to Naloxone on Loperamide-induced Delay of the Oro-cecal, Whole-gut and Colon Transit Time.

Start date: May 2011
Phase: Phase 1
Study type: Interventional

The purpose of this study is to describe the effects of repeated-dose methylnaltrexone in preventing loperamide-induced delay of whole-gut, oro-cecal and colon transit time and to measure pharmacokinetics of methylnaltrexone and naloxone-3-glucuronide after oral administration of methylnaltrexone and naloxone.

NCT ID: NCT01545063 Completed - Crohn's Disease Clinical Trials

CAre of Patients With PArenteral Nutrition At Home

CAPANAH
Start date: May 2012
Phase: N/A
Study type: Observational

This research aims to give an overview of a number of aspects related to the quality of care for adult patients on home parenteral nutrition. Concretely this study follows up different aspects on different moments in the care of the patient pathways: - process indicators concerning indication, parenteral nutrition, training, team access roads and the succession of complications - Outcome indicators - the health-related quality of life - discrepancies in medication use - the role of the different health care providers

NCT ID: NCT01524081 Completed - Acute Appendicitis Clinical Trials

Antibiotic Prophylaxis in the Prevention of Surgical Site Infections After Selected Urgent Abdominal Surgical Procedures

Start date: July 2008
Phase: Phase 3
Study type: Interventional

Aim of prospective randomized a placebo controlled study is to prove that in case of acute surgical procedure due to appendicitis, ileus of small bowel and perforation of small bowel and stomach appropriately administered antibiotic prophylaxis is effective with lower incidence of infection in surgical site and comparable risk of development of other nosocomial infections versus group without antibiotic prophylaxis. Secondary aim is to determine risk of developing nosocomial infection in the above mentioned group of patients, identify group of patients which does not benefit from prophylaxis, and compile financial costs for antibiotic prophylaxis and treatment of nosocomial infections and thus the background for the recommended procedure with regards that such prospective study does not exist in the Czech Republic.

NCT ID: NCT01507246 Completed - Bowel Obstruction Clinical Trials

Adult Patients Undergoing Open Colectomy MA402S23B303

IMPROVE-Open
Start date: December 2011
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL(R) to determine if total opioid consumption is reduced when using EXPAREL, therefore possibly reducing total hospitalization costs.

NCT ID: NCT01137201 Completed - Clinical trials for The Prevalence of Surgery for Small Bowel Obstruction After LGBP Procedure.

Internal Hernia After Laparoscopic Gastric Bypass

Start date: May 2010
Phase: N/A
Study type: Interventional

To see if closing the mesenteric defects created at a Laparoscopic Gastric Bypass is better than leaving them open.

NCT ID: NCT01102283 Completed - Colonic Obstruction Clinical Trials

Treatment of Colonic Obstruction With Cook Evolution® Colonic Stent System

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

The objective of this registry is to compile clinical data on the use of the Evolution® Colonic Stent System for the palliative treatment of colonic obstruction or strictures caused by malignant neoplasms and to relieve acute large bowel obstruction prior to colectomy in patients with malignant strictures.

NCT ID: NCT01082627 Completed - Clinical trials for Small Bowel Obstruction

Identifying the Effect of Somatostatin Treatment in Early Postoperative Simple Small Bowel Obstruction

Start date: June 2009
Phase: Phase 4
Study type: Interventional

Primary Objective: To demonstrate whether an early fixed Somatostatin treatment improves the complete recovery rate of early postoperative simple small bowel obstruction (EPSSBO) compared with the common daily practice Notes: 1. complete recovery= toleration of solid food+ flatus+ passage+ recovery of bowel movement. 2. common daily practice includes: - NPO (Nil per mouth), re-dehydration, TPN (Total Parenteral Nutrition) if needed. Check & make sure stability of electrolytes daily. - GI (Gastro-Intestinal) depression via NGT (Naso-Gastric Tube) - Discontinue opiates, instead of NSAIDs. (Non-Steroidal Anti-Inflammatory Drugs) - Pro-dynamic drugs or other drugs which may interfere with GI (Gastro-Intestinal) movement eg. anti-histamines, anti-cholinergic, opiates, anti-depressives are not indicated. Secondary Objectives: To investigate whether an early fixed Somatostatin treatment will bring much benefit to EPSSBO pts compared with the common daily practice,for this purpose,the study will investigate the endpoints below.