ID

25940

Description

Study ID: 101468/169 Clinical Study ID: 101468/169 Study Title:A Phase III, Randomised, Double-blind, Placebo-controlled, Parallel Group Study of Six Months Treatment with Ropinirole CR as Adjunctive Therapy in Patients with Parkinson's Disease who are not Optimally Controlled on L-dopa Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00381472 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Parkinson Disease This is the L-Dopa Medication form.

Keywords

  1. 9/17/17 9/17/17 -
  2. 9/28/17 9/28/17 -
Uploaded on

September 28, 2017

DOI

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License

Creative Commons BY-NC 3.0

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GSK Ropinirole in Patients Suffering from Parkinsons Disease L-Dopa Medication 101468/169 NCT00381472

GSK Ropinirole in Patients Suffering from Parkinsons Disease L-Dopa Medication 101468/169 NCT00381472

L-DOPA MEDICATION
Description

L-DOPA MEDICATION

Alias
UMLS CUI-1
C0023570
Was any L-Dopa taken by the subject during the study or within 30 days prior to the study? If Yes, record each instance below.
Description

Was any L-Dopa taken by the subject during the study or within 30 days prior to the study?

Data type

boolean

Alias
UMLS CUI [1]
C0023570
Drug Name
Description

Drug Name

Data type

text

Alias
UMLS CUI [1,1]
C0023570
UMLS CUI [1,2]
C0013227
Unit Dose
Description

Unit Dose

Data type

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0023570
UMLS CUI [1,3]
C0869039
Units
Description

Units

Data type

text

Alias
UMLS CUI [1,1]
C1519795
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0023570
Frequency
Description

Frequency

Data type

text

Alias
UMLS CUI [1,1]
C1519795
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0023570
Route
Description

Route

Data type

text

Alias
UMLS CUI [1,1]
C0013153
UMLS CUI [1,2]
C0023570
UMLS CUI [1,3]
C0013227
Reason for Medication
Description

Reason for Medication

Data type

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0023570
Start Date
Description

Start Date

Data type

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
UMLS CUI [1,3]
C0023570
Stop Date
Description

Stop Date

Data type

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0023570
Ongoing Medication?
Description

Ongoing Medication?

Data type

boolean

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C0023570

Similar models

GSK Ropinirole in Patients Suffering from Parkinsons Disease L-Dopa Medication 101468/169 NCT00381472

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
L-DOPA MEDICATION
C0023570 (UMLS CUI-1)
Was any L-Dopa taken by the subject during the study or within 30 days prior to the study?
Item
Was any L-Dopa taken by the subject during the study or within 30 days prior to the study? If Yes, record each instance below.
boolean
C0023570 (UMLS CUI [1])
Drug Name
Item
Drug Name
text
C0023570 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Unit Dose
Item
Unit Dose
text
C0013227 (UMLS CUI [1,1])
C0023570 (UMLS CUI [1,2])
C0869039 (UMLS CUI [1,3])
Item
Units
text
C1519795 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0023570 (UMLS CUI [1,3])
Code List
Units
CL Item
Tablet (TAB)
CL Item
Microlitre (MCL)
CL Item
Millilitre (ML)
CL Item
Litre (L)
CL Item
Microgram (MCG)
CL Item
Milligram (MG)
CL Item
Gram (G)
Item
Frequency
text
C1519795 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0023570 (UMLS CUI [1,3])
Code List
Frequency
CL Item
1x Daily (OD)
CL Item
2x Daily (BID)
CL Item
3x Daily (TID)
CL Item
4x Daily (QID)
CL Item
As required (PRN)
Item
Route
text
C0013153 (UMLS CUI [1,1])
C0023570 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
Code List
Route
CL Item
Intramuscular (IM)
CL Item
Inhalation (IH)
CL Item
Intravenous (IV)
CL Item
Nasal (NS)
CL Item
Topical (TP)
CL Item
Oral (PO)
CL Item
Vaginal (VG)
Reason for Medication
Item
Reason for Medication
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0023570 (UMLS CUI [1,3])
Start Date
Item
Start Date
date
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0023570 (UMLS CUI [1,3])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C0023570 (UMLS CUI [1,2])
Ongoing Medication?
Item
Ongoing Medication?
boolean
C0549178 (UMLS CUI [1,1])
C0023570 (UMLS CUI [1,2])

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