Study of Alvimopan for the Management of Opioid-induced Postoperative Bowel Dysfunction/Postoperative Ileus
Primary Purpose
Ileus
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Alvimopan
Sponsored by
About this trial
This is an interventional treatment trial for Ileus focused on measuring Postoperative ileus
Eligibility Criteria
Inclusion Criteria:
- Subject is scheduled for a partial small/large bowel resection of primary anastomosis or total abdominal hysterectomy (simple or radical) via laparotomy
- Subject is scheduled to receive primary postoperative pain management with intravenous (i.v.) patient-controlled analgesia (PCA) opioids
Exclusion Criteria:
- Subject is scheduled for a total colectomy, colostomy, ileostomy
- Subject has complete bowel obstruction
- Subject is currently taking opioid analgesics or has taken opioid analgesics within 4 weeks prior to surgery
Sites / Locations
- Various
Outcomes
Primary Outcome Measures
acceleration of gastrointestinal recovery
Secondary Outcome Measures
time until ready for discharged based upon recovery of GI function
severity of GI symptoms
pain
opioid consumption
time to tolerate solid food
need for reinsertion of nasogastric tube
time until discharge order is written
Full Information
NCT ID
NCT00388258
First Posted
October 13, 2006
Last Updated
August 17, 2017
Sponsor
Cubist Pharmaceuticals LLC
Collaborators
GlaxoSmithKline
1. Study Identification
Unique Protocol Identification Number
NCT00388258
Brief Title
Study of Alvimopan for the Management of Opioid-induced Postoperative Bowel Dysfunction/Postoperative Ileus
Official Title
A Multicenter Phase III, Double-Blind, Placebo-Controlled, Parallel Study of ADL-8-2698 in Opioid-Induced Postoperative Bowel Dysfunction/Postoperative Ileus
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
March 1, 2001 (Actual)
Primary Completion Date
December 1, 2002 (Actual)
Study Completion Date
December 1, 2002 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Cubist Pharmaceuticals LLC
Collaborators
GlaxoSmithKline
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief 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).
Detailed Description
Postoperative ileus (POI) is temporary slowing down or stopping of bowel function and a slowing down of movement of contents of the intestines. This functional impairment persists for a variable duration following surgery, usually resolving within 1 day in the small intestine, 1 to 3 days in the stomach and 3 to 5 days in the colon. When POI persists for more than 5 days, it is generally considered severe, sometimes referred to as complicated or prolonged POI, and increases the risk for related morbidity. No drug therapy has been shown to consistently shorten the duration of POI. This study is designed to demonstrate that alvimopan, a novel, peripherally acting mu opioid receptor antagonist, accelerates the recovery of GI function in patients undergoing bowel resection of hysterectomy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ileus
Keywords
Postoperative ileus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
451 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Alvimopan
Primary Outcome Measure Information:
Title
acceleration of gastrointestinal recovery
Secondary Outcome Measure Information:
Title
time until ready for discharged based upon recovery of GI function
Title
severity of GI symptoms
Title
pain
Title
opioid consumption
Title
time to tolerate solid food
Title
need for reinsertion of nasogastric tube
Title
time until discharge order is written
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subject is scheduled for a partial small/large bowel resection of primary anastomosis or total abdominal hysterectomy (simple or radical) via laparotomy
Subject is scheduled to receive primary postoperative pain management with intravenous (i.v.) patient-controlled analgesia (PCA) opioids
Exclusion Criteria:
Subject is scheduled for a total colectomy, colostomy, ileostomy
Subject has complete bowel obstruction
Subject is currently taking opioid analgesics or has taken opioid analgesics within 4 weeks prior to surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adolor Corporation
Organizational Affiliation
Cubist Pharmaceuticals LLC
Official's Role
Study Director
Facility Information:
Facility Name
Various
City
Exton
State/Province
Pennsylvania
ZIP/Postal Code
19341
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
15906123
Citation
Delaney CP, Weese JL, Hyman NH, Bauer J, Techner L, Gabriel K, Du W, Schmidt WK, Wallin BA; Alvimopan Postoperative Ileus Study Group. Phase III trial of alvimopan, a novel, peripherally acting, mu opioid antagonist, for postoperative ileus after major abdominal surgery. Dis Colon Rectum. 2005 Jun;48(6):1114-25; discussion 1125-6; author reply 1127-9. doi: 10.1007/s10350-005-0035-7.
Results Reference
result
PubMed Identifier
20526599
Citation
Ludwig K, Viscusi ER, Wolff BG, Delaney CP, Senagore A, Techner L. Alvimopan for the management of postoperative ileus after bowel resection: characterization of clinical benefit by pooled responder analysis. World J Surg. 2010 Sep;34(9):2185-90. doi: 10.1007/s00268-010-0635-9.
Results Reference
derived
Learn more about this trial
Study of Alvimopan for the Management of Opioid-induced Postoperative Bowel Dysfunction/Postoperative Ileus
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