ID
25916
Beschrijving
Study ID: 101468/196 Clinical Study ID: 101468/196 Study Title: 101468/196: A Long-Term, Open-Label Continuation Study of Once Daily Administration of Ropinirole CR Tablets to Patients with Parkinson's Disease who Completed the Previous Ropinirole CR Studies 167 or 164 Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00650104 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Parkinson DiseaseA Long-Term, Open-Label Continuation Study of Once Daily Adminstration of Ropinirole CR Tablets to Patients with Parkinson's Disease Who Completed the Previous Ropinirole CR Studies - 167 & 164 Eligibility Criteria
Trefwoorden
Versies (1)
- 27-09-17 27-09-17 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
27 september 2017
DOI
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Licentie
Creative Commons BY-NC-ND 3.0
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Eligibility Criteria Ropinirole in Parkinson's Disease GSK 101468/196
Eligibility Criteria
- StudyEvent: Study Event
Beschrijving
All responses must be NO or N/A for the patient to be enrolled in the study
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
Datatype
boolean
Alias
- UMLS CUI [1]
- C0805162
- UMLS CUI [2]
- C0805162
- UMLS CUI [3]
- C0201975
- UMLS CUI [4]
- C0438154
Datatype
text
Alias
- UMLS CUI [1]
- C0020651
Beschrijving
Epworth Sleep Score
Datatype
boolean
Alias
- UMLS CUI [1]
- C3541276
Beschrijving
Substance Use Disorder
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038586
Beschrijving
Hypersensitivity to Ropinirole
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0244821
Beschrijving
Investigational Drug
Datatype
boolean
Beschrijving
Gynaecological Status
Datatype
text
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Beschrijving
Withdrawal
Datatype
boolean
Alias
- UMLS CUI [1]
- C2349954
Beschrijving
Exclusion
Datatype
boolean
Alias
- UMLS CUI [1]
- C2828389
Similar models
Eligibility Criteria
- StudyEvent: Study Event
C0244821 (UMLS CUI [2])
C0805162 (UMLS CUI [2])
C0201975 (UMLS CUI [3])
C0438154 (UMLS CUI [4])
C0244821 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])