Clinical trial

Randomized Evaluation of the 24-Hour Coverage: Efficacy of Rotigotine

NCT00474058 · UCB Pharma, Industry · Completed

Key facts

NCT number NCT00474058
Title Randomized Evaluation of the 24-Hour Coverage: Efficacy of Rotigotine
Official title Phase 3B, Multicenter, Multinational, Double-Blind, Placebo Controlled, 2-Arm Trial to Evaluate the Effect of the 24-Hour Transdermal Delivery of Rotigotine on the Control of Early Morning Motor Function, Sleep Quality, Nocturnal Symptoms, and Non-Motor Symptoms in Subjects With Idiopathic…
Acronym RECOVER
Lead sponsor UCB Pharma, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Parkinson's Disease
Intervention type Drug, Other
Interventions Rotigotine, Placebo
Enrollment 287
Start date May 1, 2007
Primary completion Mar 1, 2009
Completion Mar 1, 2009
First posted May 16, 2007
Last update posted Jun 22, 2015
Countries Australia, Austria, Finland, Germany, Hungary, Italy, New Zealand, Poland, South Africa, Spain, United Kingdom, United States

At a glance

  • Yes Results posted
  • None Linked FDA submissions

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

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies