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Result Summary for RRL103660

Result Summary
Protocol ID: RRL103660
Clinical Study ID: RRL103660
Official Title: A 12-Week, Multi-Center, Double-Blind, Placebo-Controlled, Parallel Group, Flexible Dose Polysomnography Study of Ropinirole Controlled Release for Restless Legs Syndrome (RLS) in RLS Patients with Sleep Disturbance and Periodic Limb Movements (PLM) During Sleep
Phase: phase 4
Study Indications or Diseases:
  • Restless Legs Syndrome
Generic Name: ropinirole
Trade/Product Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara
Approved Drug Label: http://www.gsk.com/products.html
Results Summary: Click here to download result summary. Click here to download result summary.
Citations:

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