Clinical trial

RLS In Adults: Comparing Immediate Release Formulation With Extended Release…

NCT00314860 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00314860
Title RLS In Adults: Comparing Immediate Release Formulation With Extended Release Formulation Of Ropinirole
Official title A 12-Week, Randomized, Double-Blind, Parallel Group, Multicentre Study to Assess the Tolerability and Clinical Benefits of Ropinirole Extended Release (XR) Tablets Compared With Ropinirole Immediate Release (IR) Tablets in Subjects With Restless Legs Syndrome (RLS)
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Restless Legs Syndrome, Restless Legs Syndrome (RLS)
Intervention type Drug
Interventions ropinirole Extended Release (XR)
Enrollment 568
Start date Feb 1, 2006
Primary completion Dec 1, 2006
Completion Dec 1, 2006
First posted Apr 17, 2006
Last update posted Oct 18, 2016
Countries Australia, Austria, Belgium, Denmark, France, Germany, Italy, Netherlands, Norway, Spain, Sweden, United Kingdom and 1 more

At a glance

  • 10–99 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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