ID
40733
Description
Study ID: 101468/218 Clinical Study ID: SKF-101468/218 Study Title:A Single-Blind, Randomised, Placebo-Controlled, Parallel-Group, Multicentre, Phase IIa Study to Determine the Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: requip Study Indication: Restless Legs Syndrome
Keywords
Versions (1)
- 5/5/20 5/5/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
May 5, 2020
DOI
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License
Creative Commons BY-NC 4.0
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Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218
Alcohol Breath Test, Randomisation, Drug Screening
- StudyEvent: ODM
Description
Alcohol Breath Test
Alias
- UMLS CUI-1
- C0202306
Description
Was an alcohol breath test carried out?
Data type
boolean
Alias
- UMLS CUI [1]
- C0202306
Description
If no alcohol breath test was carried out, specify reason
Data type
text
Alias
- UMLS CUI [1,1]
- C0202306
- UMLS CUI [1,2]
- C2826287
Description
Date of alcohol breath test
Data type
date
Alias
- UMLS CUI [1,1]
- C0202306
- UMLS CUI [1,2]
- C0011008
Description
Result of alcohol breath test
Data type
integer
Alias
- UMLS CUI [1,1]
- C0202306
- UMLS CUI [1,2]
- C1274040
Description
Randomisation
Alias
- UMLS CUI-1
- C0034656
Description
Drug Screening (Urine)
Alias
- UMLS CUI-1
- C0202274
Description
Exact date and time of sampling
Data type
date
Alias
- UMLS CUI [1]
- C0202274
- UMLS CUI [2,1]
- C0200354
- UMLS CUI [2,2]
- C0011008
- UMLS CUI [2,3]
- C0040223
Description
Were there any contra-indicated drugs detected?
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1511790
- UMLS CUI [1,2]
- C3845816
Description
Type of Drug
Data type
text
Alias
- UMLS CUI [1]
- C0457591
Description
Drug Screening Comment
Data type
text
Alias
- UMLS CUI [1,1]
- C0202274
- UMLS CUI [1,2]
- C0947611
Similar models
Alcohol Breath Test, Randomisation, Drug Screening
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C2826287 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C0201734 (UMLS CUI [2])
C0178602 (UMLS CUI [3])
C0200354 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0040223 (UMLS CUI [2,3])
C3845816 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])