ID

27194

Description

Study ID: 101468/188 Clinical Study ID: SKF-101468/188 Study Title:A Study of the Maintained Efficacy and Safety of Ropinirole Versus Placebo in the Long Term Treatment of Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Parkinson Disease Module: Screening

Keywords

Versions (1)
  1. 11/3/17 11/3/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

November 3, 2017

DOI

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License

Creative Commons BY-NC 3.0
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GSK Ropinirole in Patients Suffering from Restless Legs Syndrome 101468/188

English

Screening

1 forms  
  1. StudyEvent: ODM
    1. Screening
Concomitant Medication
Description

Concomitant Medication

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C0035258
Drug Name (Trade Name Preferred) Concomitant Medication
Description

Drug Name Concomitant Medication

Data type

text

Alias
UMLS CUI [1,1]
C2360065
UMLS CUI [1,2]
C2347852
Total Daily Dose (e.g 500 mg) Concomitant Medication
Description

Total Daily Dose Concomitant Medication

Data type

float

Measurement units
  • mg
Alias
UMLS CUI [1,1]
C2348070
UMLS CUI [1,2]
C2347852
mg
Medical Illness / Diagnosis (or symptom in absence of diagnosis) Concomitant Medication
Description

Medical Illness / Diagnosis Concomitant Medication

Data type

text

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C2347852
UMLS CUI [1,3]
C3146298
Start Date Concomitant Medication (be as precise as possible)
Description

Start Date Concomitant Medication

Data type

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C2347852
End Date Concomitant Medication
Description

End Date Concomitant Medication

Data type

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C2347852
Continuing Concomitant Medication
Description

Continuing Concomitant Medication

Data type

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Screening

1 forms
  1. StudyEvent: ODM
    1. Screening
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Concomitant Medication
C2347852 (UMLS CUI-1)
C0035258 (UMLS CUI-2)
Drug Name Concomitant Medication
Item
Drug Name (Trade Name Preferred) Concomitant Medication
text
C2360065 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Total Daily Dose Concomitant Medication
Item
Total Daily Dose (e.g 500 mg) Concomitant Medication
float
C2348070 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Medical Illness / Diagnosis Concomitant Medication
Item
Medical Illness / Diagnosis (or symptom in absence of diagnosis) Concomitant Medication
text
C0011900 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,3])
Start Date Concomitant Medication
Item
Start Date Concomitant Medication (be as precise as possible)
date
C0808070 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
End Date Concomitant Medication
Item
End Date Concomitant Medication
date
C0806020 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Continuing Concomitant Medication
Item
Continuing Concomitant Medication
boolean
C2826666 (UMLS CUI [1])
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