Intravenous (IV) Methylnaltrexone (MNTX) in the Prevention of Post-Operative Ileus
Completed · Phase 2 · Has a placebo group
Conditions studied: Postoperative Ileus
In brief
A double-blind, randomized, parallel-group study designed to evaluate the safety and activity of IV MNTX in the treatment of Post-Operative Ileus (POI) in patients who underwent segmental colectomies via laparotomy.
Key facts
- Study ID
- NCT01367548
- Run by
- Bausch Health Americas, Inc.
- People needed
- 65
- Starts
- 2003-07-01
- Expected to finish
- 2004-12-01
- Last updated by the study team
- 2019-11-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males and females, 18 yrs or older
- Patients who have undergone a segmental colectomy
- Must be receiving opioids via IV.
You may not qualify if…
- Patients who received any experimental drug in the last 30 days
- Patients receiving spinal medication for post-operative pain relief
- Patients who have undergone operations for complications related to inflammatory bowel disease
- Patients with recent history of abdominal radiation therapy.
Where it is running
- Progenics Pharmaceuticals, Inc. — Tarrytown, New York, United States
Full record on ClinicalTrials.gov
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