ID
35680
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 cntains the Eligibility criteria form. It has to be filled in for screening.
Mots-clés
Versions (2)
- 08/03/2019 08/03/2019 -
- 15/03/2019 15/03/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
15 mars 2019
DOI
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Licence
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
Eligibility criteria
- StudyEvent: ODM
Description
Inclusion criteria
Alias
- UMLS CUI-1
- C1512693
- UMLS CUI-2
- C1516637
Description
Study Subject Participation Status
Type de données
boolean
Alias
- UMLS CUI [1]
- C2348568
Description
Informed consent
Type de données
boolean
Alias
- UMLS CUI [1]
- C0021430
Description
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
- UMLS CUI-2
- C1516637
Description
Contraceptive method
Type de données
boolean
Alias
- UMLS CUI [1]
- C0700589
Description
Positive pregnancy test
Type de données
boolean
Alias
- UMLS CUI [1]
- C0240802
Description
Comorbidity
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0443343
- UMLS CUI [2,1]
- C0443343
- UMLS CUI [2,2]
- C0012634
Similar models
Eligibility criteria
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,2])
C0443343 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])