CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed
Drug / intervention
Alvimopandrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00388401
NCT00388401Phase 3Completed

A Multicenter Phase III, Double-Blind, Placebo-Controlled, Parallel Study of ADL-8-2698 in Opioid-Induced Postoperative Bowel Dysfunction/Postoperative Ileus

Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)·interventional·Posted Oct 16, 2006·Updated Jul 20, 2015

In Brief

A Phase 3 clinical trial evaluating Alvimopan for Ileus. Completed, across 1 site.

Detailed Summary

Patients undergoing major abdominal surgery are at highest risk for developing postoperative ileus (POI), occurring in nearly all cases. Signs and symptoms of POI may include abdominal distention, bloating, persistent abdominal pain; nausea and/or vomiting; delayed passage or inability to pass flatus or stool; and inability to tolerate a solid diet. This study will test the ability of alvimopan 6 mg or 12 mg given 2 hours before the scheduled start of surgery to hasten the recovery of GI function in patients undergoing major abdominal surgery (bowel resection or abdominal hysterectomy).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIleus
CountriesUnited States
CollaboratorsGlaxoSmithKline

Timeline

Phase 3CompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 16, 2006
Enrollment StartJan 1, 2002
Primary CompletionJun 1, 2003
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 19.7 years ago

Interventions

Alvimopandrug