"MILNACIPRAN" in Subjects With Chronic Shoulder Pain

Status Completed

Clinical Trial Summary

The purpose of this study is to compare the safety and efficacy of multiple doses of "Milnacipran" to a placebo dose in subjects with Chronic Shoulder Pain.

Clinical Trial Description

16 weeks. It is planned that this study will be conducted at a single site and will enroll approximately 40 subjects over 2-4 months. At the end of the 12-week dosing period, the study drug will be discontinued and all subjects in the treatment groups and control group will be followed for an additional 4 weeks. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01289236
Study type	Interventional
Source	Delray Research Associates
Contact
Status	Completed
Phase	Phase 4
Start date	October 2009
Completion date	June 2011

View Details

See also
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