Viewing StudyNCT00472199



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Last Modification Date: 2024-10-26 @ 9:32 AM
Study NCT ID: NCT00472199
Status: COMPLETED
Last Update Posted: 2014-06-27
First Post: 2007-05-10

Brief Title: Long-term Efficacy Safety and Tolerability of Pramipexole in Patients With Idiopathic Moderate to Severe Restless Legs Syndrome RLS
Sponsor:
Organization: Boehringer Ingelheim

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 331
Enrollment Type: ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE4
Observational Models:
Time Perspective List:
Who Masked List: