ID

25766

Beschrijving

Study ID: 101468/207 Clinical Study ID: SKF-101468/207 Study Title:A double-blind, randomized, placebo-controlled, parallel-group study to investigate the tolerability of a dose-escalating regimen of ropinirole in patients suffering from Restless Legs Syndrome (RLS). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 2 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication : Restless Legs Syndrome Missing Data

Trefwoorden

  1. 18-09-17 18-09-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

18 september 2017

DOI

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Licentie

Creative Commons BY-NC-ND 3.0

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Missing Data GSK Ropinirole Restless Legs Syndrome 101468

Missing Data GSK Ropinirole Restless Legs Syndrome 101468

Patient Information
Beschrijving

Patient Information

Alias
UMLS CUI-1
C1955348
Patient Number
Beschrijving

Patient Number

Datatype

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Beschrijving

Centre Number

Datatype

text

Alias
UMLS CUI [1,1]
C0600091
UMLS CUI [1,2]
C0019994
Missing Data - Instructions: Please record below any instance where data has NOT been recorded fo the subject
Beschrijving

Missing Data - Instructions: Please record below any instance where data has NOT been recorded fo the subject

Alias
UMLS CUI-1
C0814891
Form
Beschrijving

Form

Datatype

text

Alias
UMLS CUI [1]
C1516308
Visit
Beschrijving

Visit

Datatype

text

Alias
UMLS CUI [1]
C0545082
Missing Data Point
Beschrijving

Missing Data

Datatype

text

Alias
UMLS CUI [1]
C0814891
Reason
Beschrijving

Reason

Datatype

text

Similar models

Missing Data GSK Ropinirole Restless Legs Syndrome 101468

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Patient Information
C1955348 (UMLS CUI-1)
Patient Number
Item
Patient Number
text
C1830427 (UMLS CUI [1])
Centre Number
Item
Centre Number
text
C0600091 (UMLS CUI [1,1])
C0019994 (UMLS CUI [1,2])
Item Group
Missing Data - Instructions: Please record below any instance where data has NOT been recorded fo the subject
C0814891 (UMLS CUI-1)
Form
Item
Form
text
C1516308 (UMLS CUI [1])
Visit
Item
Visit
text
C0545082 (UMLS CUI [1])
Missing Data
Item
Missing Data Point
text
C0814891 (UMLS CUI [1])
Reason
Item
Reason
text

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