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

- Multiple Sclerosis
- Completed

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

Participation criteria and map of study locations

Key Participation Requirements

Gender: Female, Male

Age group: Adult

Age Range: 18 Years to 55 Years

Trial Duration: 08/01/2005 - 02/01/2006

Phase: Phase 4

Study Type

Interventional