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Post-Operative Ileus clinical trials

View clinical trials related to Post-Operative Ileus.

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NCT ID: NCT03068975 Not yet recruiting - Clinical trials for Post Operative Ileus

Alvimopan Use in Polytraumatized Patients

Start date: April 2017
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy and safety of Alvimopan(12 mg) in recovery of bowel function in an emergency trauma setting without the pre-operative dosage in patients that will receive abdominal surgery.

NCT ID: NCT02673671 Recruiting - Clinical trials for Post-operative Ileus

G-Tech Feasibility Study for Early Detection of a Post-op Ileus

Start date: February 2016
Phase: N/A
Study type: Interventional

A feasibility study for assessing and recording myoelectric activity in patients for early detection of a post-operative ileus (POI) in patients who undergo gastrointestinal surgery and differentiating the myoelectric signals from those who have normal post-operative return of GI function.

NCT ID: NCT02065583 Recruiting - Clinical trials for Post Operative Ileus

Predictive Validity of Acoustic Gastrointestinal Surveillance (AGIS) in Post-Operative Feeding

Start date: December 2013
Phase: N/A
Study type: Observational

This study will measure the accuracy of a disposable, non-invasive device for the continuous monitoring of abdominal sounds, called the AGIS sensor (Acoustic Gastro-Intestinal Surveillance) in predicting patients' intolerance to feeding (defined as severe nausea, vomiting, or need to place a nasogastric tube within 4 hours of initiating a standard feeding protocol) following abdominal surgery. This will be a pragmatic, observational study.

NCT ID: NCT01869231 Completed - Clinical trials for Post-operative Ileus

Evaluating the Efficacy of Current Treatments for Reducing Postoperative Ileus

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

Aim was to investigate efficacy of current treatments - water, chewing gum, and olive oil, in resolving postoperative ileus.

NCT ID: NCT01662115 Terminated - Clinical trials for Post-operative Ileus

Nicotine Gum Recovery After Colorectal Surgery

Start date: August 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate whether the use of nicotine gum in the postoperative period influences surgical outcome in patients undergoing colorectal surgery.

NCT ID: NCT01583452 Completed - Clinical trials for Post Operative Ileus

Chewing Gum Use to Reduce Post-operative Ileus in Pediatric Patients

Start date: April 2012
Phase: Phase 1
Study type: Interventional

Post- operative ileus refers to the time after surgery before coordinated electromotor bowel function resumes. It's treatment and prevention may signify an elevated hospitalization cost and the exposure to the patient to adverse effects of drugs. The current clinical trial has as primary objective to prove the efficacy of chewing gum as a preventive measure of post-operative ileus in pediatric patients after gastrointestinal surgery through the determination of the time the patient takes to tolerate oral intake, pass flatus, present bowel movements and the time of hospital stay. Patients will be assigned either to the case group (chewing gum + standard treatment) or to the control group (standard treatment), in both of them time from the end of surgery to the moment the patient presents first bowel movement, passes flatus, tolerates oral intake (any type of food) and is discharged from hospital; will be measured in hours and then analyzed to determine the validity of these data.

NCT ID: NCT00443040 Terminated - Clinical trials for Post-Operative Ileus

Asimadoline for the Treatment of Post-Operative Ileus

Start date: January 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of asimadoline in patients who have undergone a laparoscopic segmental colectomy and determine whether it reduces the time to recovery of bowel function compared to placebo.