ID

25688

Description

Study part: Efficacy Status (SUBJEFF). A 52-Week, Open-Label Study to Assess the Long-Term Safety of Ropinirole Extended Release (XR) in Patients with Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Clinicaltrials.gov Identifier: NCT00355641. Phase: phase 3. Study Recruitment Status: Completed. Generic Name: ropinirole. Trade Name Modutab, ZIPEREVE, ZEPREVE, REPREVE, ADARTREL, REQUIP, Zygara; Zygara, ZIPEREVE, ZEPREVE, Requip Depot, REQUIP, REPREVE, Modutab, ADARTREL. Study Indication : Restless Legs Syndrome. Study ID: 101468/206. Clinical Study ID: 101468/206.

Keywords

  1. 9/9/17 9/9/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 9, 2017

DOI

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License

Creative Commons BY-NC 3.0

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Efficacy Status (SUBJEFF) Ropinirole Restless Legs Syndrom NCT00355641

Efficacy Status (SUBJEFF)

Efficacy Status (SUBJEFF)
Description

Efficacy Status (SUBJEFF)

Alias
UMLS CUI-1
C1707887
1. Which visit will the subject be attending next?
Description

visit

Data type

text

Alias
UMLS CUI [1]
C0545082

Similar models

Efficacy Status (SUBJEFF)

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Efficacy Status (SUBJEFF)
C1707887 (UMLS CUI-1)
Item
1. Which visit will the subject be attending next?
text
C0545082 (UMLS CUI [1])
Code List
1. Which visit will the subject be attending next?
CL Item
Week 5 (Week 5)
CL Item
Week 6 (Week 6)
CL Item
Week 8 (Week 8)

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