ID
40515
Beschrijving
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
Trefwoorden
Versies (2)
- 29-04-20 29-04-20 -
- 08-05-20 08-05-20 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
29 april 2020
DOI
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Licentie
Creative Commons BY-NC 4.0
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Pharmacokinetics and Tolerability of Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/218
Dose Level 1, Day1 - Vital Signs Post Dose; Adverse Event
- StudyEvent: ODM
Beschrijving
Adverse Event
Alias
- UMLS CUI-1
- C0877248
Beschrijving
If "Yes" record all details on an Adverse Event page at back of CRF.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0877248
Beschrijving
If "Yes" record all details on an Adverse Event page at back of CRF.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0877248
Beschrijving
Y - Ensure patient returns home with their study medication and diary card N - Select a dosing strategy from options below and tick the relevant box
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0805733
- UMLS CUI [1,2]
- C2603343
- UMLS CUI [1,3]
- C4534363
Beschrijving
If it is not safe for the patient to continue dosing at home, select a dosing strategy from options below and tick the relevant
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0805733
- UMLS CUI [1,2]
- C2603343
- UMLS CUI [1,3]
- C4534363
- UMLS CUI [2,1]
- C0178602
- UMLS CUI [2,2]
- C0679199
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Dose Level 1, Day1 - Vital Signs Post Dose; Adverse Event
- StudyEvent: ODM
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C4534363 (UMLS CUI [1,3])
C2603343 (UMLS CUI [1,2])
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