ID

25766

Description

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

Keywords

Versions (1)
  1. 9/18/17 9/18/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 18, 2017

DOI

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License

Creative Commons BY-NC-ND 3.0
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Missing Data GSK Ropinirole Restless Legs Syndrome 101468

English

Missing Data GSK Ropinirole Restless Legs Syndrome 101468

1 forms  
Patient Information
Description

Patient Information

Alias
UMLS CUI-1
C1955348
Patient Number
Description

Patient Number

Data type

text

Alias
UMLS CUI [1]
C1830427
Centre Number
Description

Centre Number

Data type

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
Description

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

Alias
UMLS CUI-1
C0814891
Form
Description

Form

Data type

text

Alias
UMLS CUI [1]
C1516308
Visit
Description

Visit

Data type

text

Alias
UMLS CUI [1]
C0545082
Missing Data Point
Description

Missing Data

Data type

text

Alias
UMLS CUI [1]
C0814891
Reason
Description

Reason

Data type

text

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Similar models

Missing Data GSK Ropinirole Restless Legs Syndrome 101468

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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