ID
29072
Beschrijving
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)
Trefwoorden
Versies (1)
- 23-02-18 23-02-18 -
Houder van rechten
GlaxoSmithKline (GSK)
Geüploaded op
23 februari 2018
DOI
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Licentie
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
Beschrijving
Please complete the following exclusion criteria.
Alias
- UMLS CUI-1
- C0680251
Beschrijving
RLS Symptoms
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0035258
- UMLS CUI [1,2]
- C1457887
- UMLS CUI [1,3]
- C0332169
Beschrijving
Sleep disorders
Datatype
boolean
Alias
- UMLS CUI [1]
- C0851578
Beschrijving
Movement disorders
Datatype
boolean
Alias
- UMLS CUI [1]
- C0026650
Beschrijving
Comorbidity affecting efficacy
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0392760
- UMLS CUI [1,3]
- C0087111
Beschrijving
Ropinirole intolerance
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1744706
- UMLS CUI [1,2]
- C0244821
Beschrijving
Substance abuse/dependence
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0038586
- UMLS CUI [1,2]
- C0038580
Beschrijving
Contraception
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0700589
- UMLS CUI [1,2]
- C0332197
Beschrijving
Pregnancy or breast feeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Beschrijving
Unstable medical conditions
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3843040
- UMLS CUI [1,2]
- C0443343
Beschrijving
Compliance behavior
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0439801
Beschrijving
Blood pressure
Datatype
boolean
Alias
- UMLS CUI [1]
- C0005823
Beschrijving
Participation in other clinical trials
Datatype
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])