Study to Evaluate the Impact of Using Warm Compress Prior to Daily Injections of Copaxone®

Study Title

A Study to Evaluate the Impact of Using Warm Compress Prior to Daily Injections of Copaxoneֲ®

Teva Identifier

PM016

ClinicalTrials.gov Identifier

NCT00239993

Study Status

Completed

Trial Condition(s)

Multiple Sclerosis

Interventions

Drug: glatiramer acetate | Procedure: Warm compress prior to injection of glatiramer acetate

Study Description

Please refer to ClinicalTrials.gov for a description of the trial
ClinicalTrials.gov study records with inclusion and exclusion criteria
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Key Participation Requirements

Gender

Female, Male

Age Range

18 Years to 55 Years

Trial Duration

08/01/2005 - 02/01/2006

Phase

Phase 4

Study Type

Interventional