ID

40756

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

  1. 08-05-20 08-05-20 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

8 mei 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 Details

  1. StudyEvent: ODM
    1. Dose Details
Dose Details
Beschrijving

Dose Details

Alias
UMLS CUI-1
C0678766
UMLS CUI-2
C1522508
Number of Tablets:
Beschrijving

Number of Tablets:

Datatype

integer

Alias
UMLS CUI [1,1]
C0805077
UMLS CUI [1,2]
C0039225
Dose Level:
Beschrijving

Dose Level:

Datatype

integer

Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0441889
Dose Details - Comments
Beschrijving

Dose Details - Comments

Datatype

text

Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C1522508
UMLS CUI [2]
C0947611
Dose checked and administered by
Beschrijving

Dose checked and administered by

Datatype

text

Alias
UMLS CUI [1,1]
C1283174
UMLS CUI [1,2]
C0178602
UMLS CUI [2]
C2348343
Dose checked and witnessed by
Beschrijving

Dose checked and witnessed by

Datatype

text

Alias
UMLS CUI [1,1]
C1283174
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0682356
UMLS CUI [2,2]
C0178602

Similar models

Dose Details

  1. StudyEvent: ODM
    1. Dose Details
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Dose Details
C0678766 (UMLS CUI-1)
C1522508 (UMLS CUI-2)
Number of Tablets:
Item
Number of Tablets:
integer
C0805077 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Dose Level:
Item
Dose Level:
integer
C0678766 (UMLS CUI [1,1])
C0441889 (UMLS CUI [1,2])
Dose Details - Comments
Item
Dose Details - Comments
text
C0678766 (UMLS CUI [1,1])
C1522508 (UMLS CUI [1,2])
C0947611 (UMLS CUI [2])
Dose checked and administered by
Item
Dose checked and administered by
text
C1283174 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C2348343 (UMLS CUI [2])
Dose checked and witnessed by
Item
Dose checked and witnessed by
text
C1283174 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0682356 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])

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