Specified Drug Use-Results Survey of Regnite

Status Completed

Clinical Trial Summary

This study is to investigate the long-term safety and efficacy and the information on the proper use of Regnite® under conditions of daily clinical use.

Clinical Trial Description

Sleeping condition and severity of restless legs syndrome (RLS) were recorded at the start and during the treatment. The treatment period is scheduled to last 52 weeks in principle. For patients completing or discontinuing the use of Regnite® within 52 weeks, follow up on the withdrawal and rebound syndrome will be conducted up to 4 weeks of completion or discontinuation. ;

Study Design

Related Conditions & MeSH terms

Restless Legs Syndrome

Clinical Trial Details

NCT number	NCT01887613
Study type	Observational
Source	Astellas Pharma Inc
Contact
Status	Completed
Phase
Start date	October 1, 2012
Completion date	February 28, 2019

View Details

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