ID
35683
Description
Study ID: 101468/192 Clinical Study ID: 101468/192 Study Title:A 52 Week Open-Label Extension Study of the Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A 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 The study consists of 16 visits which are devided in 3 study books: Book 1: Screening (+Baseline), Day 2, Week 1, Week 2 , Week 3 , Week 4, Week 5, Week 6, Week 7, Week 8 Book 2: Week 12, Week 24, Week 36, Week 48, Week 52, Follow-up Book 3: Early withdrawal and Follow-up Each follow-up Visit takes place 7 +/- 3 days after last dose This document contains the Mos-sleep, WPAI RLS Score, SF-36 (health status questionaire)and RLS Quality Of Life Questionnaire form. It has to be filled in for Baseline, Week 12, Week 24, Week 36, Week 48 and early withdrawal.
Keywords
Versions (1)
- 3/15/19 3/15/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
March 15, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS), 101468/192
MOS – SLEEP, WPAI RLS Score, SF-36 (health status questionaire), RLS Quality Of Life Questionnaire
Description
Mos-sleep Questionnaire
Alias
- UMLS CUI-1
- C0034394
Description
Work productivity and activity impairment questionaire - Restless Legs Syndrome (WPAI-(RLS))
Alias
- UMLS CUI-1
- C3639722
Description
SF-36 (Health status questionaire)
Alias
- UMLS CUI-1
- C1519136
Description
RLS Quality Of Life Questionnaire
Alias
- UMLS CUI-1
- C0034394
- UMLS CUI-2
- C0034380
- UMLS CUI-3
- C0679830
- UMLS CUI-4
- C0035258
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