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Clinical Trial Summary

To determine the efficacy of subcutaneous MNTX to relieve opioid-induced constipation in patients with advanced medical illness.


Clinical Trial Description

This is a multi-center, double-blind, randomized parallel group study conducted in patients with advanced medical illness and opioid-induced constipation. Eligible patients are randomly assigned to receive SC doses of either MNTX, dose 1 or placebo every other day for 2 weeks. At Day 8, eligible patients, if allowed, could be escalated to a a higher dose of MNTX. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00402038
Study type Interventional
Source Bausch Health Americas, Inc.
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Status Completed
Phase Phase 3
Start date February 2004
Completion date October 2005