ID
29072
Description
Study ID: 101468/249 Clinical Study ID: 101468/249 Study Title: A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00363857 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: N/A 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; Restless Legs Syndrome (RLS)
Keywords
Versions (1)
- 2/23/18 2/23/18 -
Copyright Holder
GlaxoSmithKline (GSK)
Uploaded on
February 23, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Clinical Study, Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS), Study ID: 101468/249, NCT00363857
Eligibility Check
- StudyEvent: ODM
Description
Please complete the following exclusion criteria.
Alias
- UMLS CUI-1
- C0680251
Description
RLS Symptoms
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0035258
- UMLS CUI [1,2]
- C1457887
- UMLS CUI [1,3]
- C0332169
Description
Sleep disorders
Data type
boolean
Alias
- UMLS CUI [1]
- C0851578
Description
Movement disorders
Data type
boolean
Alias
- UMLS CUI [1]
- C0026650
Description
Comorbidity affecting efficacy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0392760
- UMLS CUI [1,3]
- C0087111
Description
Ropinirole intolerance
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1744706
- UMLS CUI [1,2]
- C0244821
Description
Substance abuse/dependence
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0038586
- UMLS CUI [1,2]
- C0038580
Description
Contraception
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0700589
- UMLS CUI [1,2]
- C0332197
Description
Pregnancy or breast feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Unstable medical conditions
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3843040
- UMLS CUI [1,2]
- C0443343
Description
Compliance behavior
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0439801
Description
Blood pressure
Data type
boolean
Alias
- UMLS CUI [1]
- C0005823
Description
Participation in other clinical trials
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C0008976
Similar models
Eligibility Check
- StudyEvent: ODM
C0035258 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,2])
C0332169 (UMLS CUI [1,3])
C0392760 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0244821 (UMLS CUI [1,2])
C0038580 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0443343 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,2])