Status:

COMPLETED

Efficacy and Safety of Pramipexole Compared to Placebo in the Treatment of Restless Legs Syndrome (RLS)

Lead Sponsor:

Boehringer Ingelheim

Conditions:

Restless Legs Syndrome

Eligibility:

All Genders

18-80 years

Phase:

PHASE3

Brief Summary

A 12 week clinical trial was conducted in the United States in order to compare pramipexole (Mirapex®) versus placebo for the ability to reduce the symptoms of restless legs syndrome in adult subjects...

Eligibility Criteria

Inclusion

    Exclusion

      Key Trial Info

      Start Date :

      April 1 2004

      Trial Type :

      INTERVENTIONAL

      Allocation :

      ACTUAL

      End Date :

      February 1 2005

      Estimated Enrollment :

      345 Patients enrolled

      Trial Details

      Trial ID

      NCT00133198

      Start Date

      April 1 2004

      End Date

      February 1 2005

      Last Update

      November 8 2013

      Active Locations (44)

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      Page 1 of 11 (44 locations)

      1

      Pivotal Research Centers

      Peoria, Arizona, United States, 85381

      2

      Mayo Clinic - Scottsdale

      Scottsdale, Arizona, United States, 85259

      3

      Boehringer Ingelheim Investigational Site

      Fountain Valley, California, United States, 92708

      4

      HealthQuest Clinical Trials Research

      San Diego, California, United States, 92123

      Efficacy and Safety of Pramipexole Compared to Placebo in the Treatment of Restless Legs Syndrome (RLS) | DecenTrialz