ID
26064
Beschrijving
Exclusion Criteria 1 Ropinirole Case Report Study ID: 100013 Clinical Study ID: RRL100013 A 12-Week, Double-Blind, Placebo-Controlled, Twice-Daily Dosing Study to Assess the Efficacy and Safety of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Requiring Extended Treatment Coverage
Trefwoorden
Versies (1)
- 05-10-17 05-10-17 -
Houder van rechten
gsk
Geüploaded op
5 oktober 2017
DOI
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Licentie
Creative Commons BY-NC 3.0
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Exclusion Criteria 1 Ropinirole Case Report Form GSK RRL100013
Exclusion Criteria 1 Ropinirole Case Report Form GSK RRL100013
- StudyEvent: ODM
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Beschrijving
Adverse reaction to study drug
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0559546
- UMLS CUI [1,2]
- C0013175
Beschrijving
Abnormality of organs or blood
Datatype
boolean
Alias
- UMLS CUI [1]
- C0243050
- UMLS CUI [2]
- C0027765
- UMLS CUI [3]
- C0004936
- UMLS CUI [4]
- C0475182
- UMLS CUI [5]
- C0151746
Beschrijving
Postural hypotension or faints
Datatype
boolean
Alias
- UMLS CUI [1]
- C0020651
- UMLS CUI [2]
- C0039070
Beschrijving
Gastrointestinal, hepatic or renal disease
Datatype
boolean
Alias
- UMLS CUI [1]
- C0017178
- UMLS CUI [2]
- C0023895
- UMLS CUI [3]
- C0022658
- UMLS CUI [4]
- C1512073
Beschrijving
Subjects who have taken OTC medication (apart from CYP1A2 medications, see below) may still be entered into the study, if, in the opinion of the Principal/Co-investigator in agreement with the Sponsor, the medication received will not interfere with the study procedures or compromise subject1s safety.
Datatype
boolean
Alias
- UMLS CUI [1]
- C3166216
- UMLS CUI [2]
- C0013231
- UMLS CUI [3,1]
- C4054723
- UMLS CUI [3,2]
- C0008972
Beschrijving
Drugs with effect on CYP1A2
Datatype
boolean
Alias
- UMLS CUI [1]
- C1827490
- UMLS CUI [2,1]
- C0919438
- UMLS CUI [2,2]
- C0207509
Similar models
Exclusion Criteria 1 Ropinirole Case Report Form GSK RRL100013
- StudyEvent: ODM
C0013175 (UMLS CUI [1,2])
C0027765 (UMLS CUI [2])
C0004936 (UMLS CUI [3])
C0475182 (UMLS CUI [4])
C0151746 (UMLS CUI [5])
C0039070 (UMLS CUI [2])
C0023895 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C1512073 (UMLS CUI [4])
C0013231 (UMLS CUI [2])
C4054723 (UMLS CUI [3,1])
C0008972 (UMLS CUI [3,2])
C0919438 (UMLS CUI [2,1])
C0207509 (UMLS CUI [2,2])