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Intestinal Obstruction clinical trials

View clinical trials related to Intestinal Obstruction.

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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: NCT01669044 Recruiting - Cirrhosis Clinical Trials

Comparison the Hemodynamics Effects Between Dexmedetomidine and Propofol in Major Abdominal Surgical Patients

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

The alpha2 agonist dexmedetomidine is a new sedative agent combined with the analgesic qualities and lack of respiratory depression. Patients sedated with dexmedetomidine could be easily roused, these advances shows dexmedetomidine may be a effective and safe sedative agent. But some studies showed some adversely effects of dexmedetomidine on haemodynamics (such as bradycardia, hypotension), the investigators want to further research the effects of dexmedetomidine on haemodynamics, such as Cardiac Output (CO), Systemic Venous Resistance Index(SVRI), and so on. Propofol is widely used sedative agent in ICU, it also has adversely effects like bradycardia and hypotension, so the investigators want to compare the effect of dexmedetomidine with propofol on haemodynamics after major abdominal surgery. Expect to further research the mechanism of haemodynamics of dexmedetomidine.

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: NCT01561729 Recruiting - Clinical trials for Gastrointestinal Hemorrhage

Nasogastric/Orogastric Tube Placement Verification Study Using RightSpot pH Indicator to Verify Gastric Acidity

Start date: January 2012
Phase: N/A
Study type: Interventional

This study will evaluate the use of RightBio Metrics' RightSpot device used to determine if there is proper placement of a nasogastric or orogastric tube.

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: NCT01507233 Terminated - Bowel Obstruction Clinical Trials

A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B302

IMPROVE-Open
Start date: May 2012
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL (bupivacaine liposome extended-release injectable suspension) to determine if total opioid consumption is reduced when using EXPAREL, therefore possibly reducing total hospitalization costs.

NCT ID: NCT01507220 Terminated - Bowel Obstruction Clinical Trials

A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B301

IMPROVE-Open
Start date: March 2012
Phase: Phase 4
Study type: Interventional

This study is designed to compare the standard of care against EXPAREL (bupivacaine liposome extended-release injectable suspension) to determine if total opioid consumption is reduced when using EXPAREL therefore possibly reducing total hospitalization costs.