Pregabalin for Abdominal Pain From Adhesions

Status Terminated

Clinical Trial Summary

The purpose of this study is to evaluate if pregabalin demonstrates significant reduction in abdominal pain from adhesions.

Clinical Trial Description

The study will be prospective, double-blinded and randomized. The study will run for 12 weeks. During the first 7 weeks there will be 2 groups in the study with subjects receiving a placebo or the study drug. During the last 4 weeks of the study, all subjects will be offered the study medication, pregabalin. The primary outcome measure will be pain relief documented by a 2-point change on the Likert pain scale with a secondary pain measure of sleep interruption. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00310765
Study type	Interventional
Source	Henry Ford Health System
Contact
Status	Terminated
Phase	Phase 4
Start date	March 2006
Completion date	August 2008

View Details

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