ID

26226

Description

Study ID: 101468/196 Clinical Study ID: 101468/196 Study Title: 101468/196: A Long-Term, Open-Label Continuation Study of Once Daily Administration of Ropinirole CR Tablets to Patients with Parkinson's Disease who Completed the Previous Ropinirole CR Studies 167 or 164 Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00650104 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 DiseaseA Long-Term, Open-Label Continuation Study of Once Daily Adminstration of Ropinirole CR Tablets to Patients with Parkinson's Disease Who Completed the Previous Ropinirole CR Studies - 167 & 164 Follow-Up

Keywords

Versions (1)
  1. 10/12/17 10/12/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

October 12, 2017

DOI

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License

Creative Commons BY-NC-ND 3.0
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Follow-Up Ropinirole in Parkinson's Disease GSK 101468/196

English

Follow-Up Ropinirole in Parkinson's Disease GSK 101468/196

1 forms  
Patient Information
Description

Patient Information

Alias
UMLS CUI-1
C1955348
Patient No.
Description

Patient Number

Data type

text

Alias
UMLS CUI [1]
C1830427
Date of Visit
Description

Date of Visit

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1320303
dd-mmm-yyyy
Orthostatic Blood Pressure/ Pulse
Description

Orthostatic Blood Pressure/ Pulse

Alias
UMLS CUI-1
C1095971
Time Point (Time [24-hour clock])
Description

Time of Examination

Data type

time

Measurement units
  • 24hr:min
Alias
UMLS CUI [1,1]
C0040223
UMLS CUI [1,2]
C0430022
24hr:min
Semi-Supine Heart Rate
Description

Semi-Supine Heart Rate

Data type

float

Measurement units
  • bpm
Alias
UMLS CUI [1,1]
C0522019
UMLS CUI [1,2]
C0018810
bpm
Standing Heart Rate
Description

Erect Heart Rate

Data type

float

Measurement units
  • bpm
Alias
UMLS CUI [1,1]
C0522014
UMLS CUI [1,2]
C0018810
bpm
Semi-Supine Systolic Blood Pressure
Description

Semi-Supine Systolic Blood Pressure

Data type

float

Measurement units
  • mmHg
Alias
UMLS CUI [1]
C0871470
mmHg
Semi-Supine Diastolic Blood Pressure
Description

Semi-Supine Diastolic Blood Pressure

Data type

float

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0522019
UMLS CUI [1,2]
C0428883
mmHg
Standing Systolic Blood Pressure
Description

Erect Systolic Blood Pressure

Data type

float

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0522014
UMLS CUI [1,2]
C0871470
mmHg
Standing Diastolic Blood Pressure
Description

Erect Diastolic Blood Pressure

Data type

float

Measurement units
  • mmHg
Alias
UMLS CUI [1,1]
C0522014
UMLS CUI [1,2]
C0428883
mmHg
Study Drug Compliance
Description

Study Drug Compliance

Alias
UMLS CUI-1
C1321605
Total number of tablets dispensed at last visit.
Description

Split up in groups of 2, 3, 4 or 8 mg.

Data type

text

Alias
UMLS CUI [1]
C0805077
Total Number of tablets returned at visit.
Description

Split up in groups of 2, 3, 4 or 8mg.

Data type

text

Alias
UMLS CUI [1]
C2699071
Number of tablets patient should have taken (assuming 100% compliance).
Description

Compliance

Data type

text

Alias
UMLS CUI [1]
C1321605
If there were missed doses, please record. Date
Description

Missed Dose: Date

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1,1]
C1709043
UMLS CUI [1,2]
C0011008
dd-mmm-yyyy
If there were missed doses, please record. Tablet(s)
Description

Missed Dose: Tablet

Data type

text

Alias
UMLS CUI [1,1]
C1709043
UMLS CUI [1,2]
C0039225
If there were missed doses, please record. Dose in mg
Description

Missed Dose: Dosage

Data type

float

Measurement units
  • mg
Alias
UMLS CUI [1,1]
C1709043
UMLS CUI [1,2]
C0178602
mg
If there were missed doses, please record. Reason
Description

Missed Dose: Reason

Data type

text

Alias
UMLS CUI [1,1]
C1709043
UMLS CUI [1,2]
C0566251
Pregnancy Test (betaHCG)
Description

Pregnancy Test (betaHCG)

Alias
UMLS CUI-1
C0032976
Was a pregnancy test performed?
Description

Pregnancy Test

Data type

integer

Alias
UMLS CUI [1]
C0032976
If YES, what type of pregnancy was performed?
Description

Type of Pregnancy Test

Data type

integer

Alias
UMLS CUI [1,1]
C0032976
UMLS CUI [1,2]
C0332307
If YES, Date of Test:
Description

Date of Pregnancy Test

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1,1]
C0032976
UMLS CUI [1,2]
C0011008
dd-mmm-yyyy
If YES, Result:
Description

Pregnancy Test Finding

Data type

integer

Alias
UMLS CUI [1]
C0427777
Completion of Dosing Period
Description

Completion of Dosing Period

Alias
UMLS CUI-1
C0805732
UMLS CUI-2
C0178602
Did the patient complete the maintenance period?
Description

Competion of maintenance period

Data type

boolean

Alias
UMLS CUI [1,1]
C0805732
UMLS CUI [1,2]
C0677908
If the answer to the question is NO, check the one most significant reason below. Adverse Event
Description

Adverse Event

Data type

integer

Alias
UMLS CUI [1]
C0877248
If the answer to the question is NO, check the one most significant reason below. Adverse event, specify:
Description

Adverse Event: Specification

Data type

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C2348235
If the answer to the question is NO, check the one most significant reason below. Patient Request.
Description

Patient Request

Data type

integer

Alias
UMLS CUI [1]
C0332153
If the answer to the question is NO, check the one most significant reason below. Patient request (unrelated to an AE), specify:
Description

Patient Request: Specification

Data type

text

Alias
UMLS CUI [1,1]
C0332153
UMLS CUI [1,2]
C2348235
If the answer to the question is NO, check the one most significant reason below. Non-compliance.
Description

Compliance

Data type

integer

Alias
UMLS CUI [1]
C1321605
If the answer to the question is NO, check the one most significant reason below. Non-compliance (unrelated to an AE), specify:
Description

Compliance: Specification

Data type

text

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C2348235
If the answer to the question is NO, check the one most significant reason below. Investigator judgement.
Description

Judgement

Data type

integer

Alias
UMLS CUI [1]
C0022423
If the answer to the question is NO, check the one most significant reason below. Investigator judgement, specify:
Description

Judgement: Specification

Data type

text

Alias
UMLS CUI [1,1]
C0022423
UMLS CUI [1,2]
C2348235
If the answer to the question is NO, check the one most significant reason below. Termination of patient dosing by sponsor.
Description

Termination

Data type

integer

Alias
UMLS CUI [1]
C0871548
If the answer to the question is NO, check the one most significant reason below. Protocol Violation.
Description

Protocol Violation

Data type

integer

Alias
UMLS CUI [1]
C1709750
If the answer to the question is NO, check the one most significant reason below. Protocol violation, specify:
Description

Protocol Violation: Specification

Data type

text

Alias
UMLS CUI [1,1]
C1709750
UMLS CUI [1,2]
C2348235
If the answer to the question is NO, check the one most significant reason below. Death; complete the Patient Death CRF.
Description

Death

Data type

integer

Alias
UMLS CUI [1]
C0011065
If the answer to the question is NO, check the one most significant reason below. Other.
Description

Other Reason

Data type

integer

Alias
UMLS CUI [1]
C3840932
If the answer to the question is NO, check the one most significant reason below. Other, specify:
Description

Other Reason: Specification

Data type

text

Alias
UMLS CUI [1,1]
C3840932
UMLS CUI [1,2]
C2348235
Date of study termination (last protocol assessment):
Description

End Date

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C0806020
dd-mmm-yyyy
Last dose in maintenance period:
Description

Last Dosage

Data type

float

Measurement units
  • mg
Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C1517741
mg
Date of last dose in maintenance period:
Description

Date of Last Dose

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1762893
dd-mmm-yyyy
Was the patient down-titrated for 1 week?
Description

Down Titration

Data type

boolean

Alias
UMLS CUI [1,1]
C2983683
UMLS CUI [1,2]
C0205216
Was the patient down-titrated for 1 week? If NO, please specify reason:
Description

Down Titration: Reason

Data type

text

Alias
UMLS CUI [1,1]
C2983683
UMLS CUI [1,2]
C0205216
UMLS CUI [1,3]
C0566251
Was the patient down-titrated for 1 week? If NO, specify duration of Down Titrationn:
Description

Down Titration: Duration

Data type

text

Alias
UMLS CUI [1,1]
C2983683
UMLS CUI [1,2]
C0205216
UMLS CUI [1,3]
C0449238
Last dose in Down-Titration:
Description

Down Titration: Last Dosage

Data type

float

Measurement units
  • mg
Alias
UMLS CUI [1,1]
C2983683
UMLS CUI [1,2]
C0205216
UMLS CUI [1,3]
C0178602
UMLS CUI [1,4]
C1517741
mg
Date of last Down-Titration Dose:
Description

Down Titration: Date of Last Dose

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1,1]
C2983683
UMLS CUI [1,2]
C0205216
UMLS CUI [1,3]
C1762893
dd-mmm-yyyy
Investigator Signature
Description

Investigator Signature

Alias
UMLS CUI-1
C2346576
To be completed by the Principal Investigator: I have assumed responsibility for completeness and accuracy of all data recorded on these Maintenance and Follow-Up Period Case Report Forms. Signature
Description

Investigator's Signature

Data type

text

Alias
UMLS CUI [1]
C2346576
To be completed by the Principal Investigator: I have assumed responsibility for completeness and accuracy of all data recorded on these Maintenance and Follow-Up Period Case Report Forms. Print Name:
Description

Investigator's Name

Data type

text

Alias
UMLS CUI [1]
C2826892
Date
Description

Date of Report

Data type

date

Measurement units
  • dd-mmm-yyyy
Alias
UMLS CUI [1]
C1302584
dd-mmm-yyyy
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Similar models

Follow-Up Ropinirole in Parkinson's Disease GSK 101468/196

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient Information
C1955348 (UMLS CUI-1)
Patient Number
Item
Patient No.
text
C1830427 (UMLS CUI [1])
Date of Visit
Item
Date of Visit
date
C1320303 (UMLS CUI [1])
Item Group
Orthostatic Blood Pressure/ Pulse
C1095971 (UMLS CUI-1)
Time of Examination
Item
Time Point (Time [24-hour clock])
time
C0040223 (UMLS CUI [1,1])
C0430022 (UMLS CUI [1,2])
Semi-Supine Heart Rate
Item
Semi-Supine Heart Rate
float
C0522019 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
Erect Heart Rate
Item
Standing Heart Rate
float
C0522014 (UMLS CUI [1,1])
C0018810 (UMLS CUI [1,2])
Semi-Supine Systolic Blood Pressure
Item
Semi-Supine Systolic Blood Pressure
float
C0871470 (UMLS CUI [1])
Semi-Supine Diastolic Blood Pressure
Item
Semi-Supine Diastolic Blood Pressure
float
C0522019 (UMLS CUI [1,1])
C0428883 (UMLS CUI [1,2])
Erect Systolic Blood Pressure
Item
Standing Systolic Blood Pressure
float
C0522014 (UMLS CUI [1,1])
C0871470 (UMLS CUI [1,2])
Erect Diastolic Blood Pressure
Item
Standing Diastolic Blood Pressure
float
C0522014 (UMLS CUI [1,1])
C0428883 (UMLS CUI [1,2])
Item Group
Study Drug Compliance
C1321605 (UMLS CUI-1)
Dispensed Amount
Item
Total number of tablets dispensed at last visit.
text
C0805077 (UMLS CUI [1])
Returned Amount
Item
Total Number of tablets returned at visit.
text
C2699071 (UMLS CUI [1])
Compliance
Item
Number of tablets patient should have taken (assuming 100% compliance).
text
C1321605 (UMLS CUI [1])
Missed Dose: Date
Item
If there were missed doses, please record. Date
date
C1709043 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Missed Dose: Tablet
Item
If there were missed doses, please record. Tablet(s)
text
C1709043 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Missed Dose: Dosage
Item
If there were missed doses, please record. Dose in mg
float
C1709043 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Missed Dose: Reason
Item
If there were missed doses, please record. Reason
text
C1709043 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Item Group
Pregnancy Test (betaHCG)
C0032976 (UMLS CUI-1)
Item
Was a pregnancy test performed?
integer
C0032976 (UMLS CUI [1])
Pregnancy Test
Code List
Was a pregnancy test performed?
CL Item
Yes (1)
CL Item
No (2)
CL Item
NA (male or female not of childbearing potential) (3)
Item
If YES, what type of pregnancy was performed?
integer
C0032976 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Type of Pregnancy Test
Code List
If YES, what type of pregnancy was performed?
CL Item
Serum (1)
CL Item
Urine (2)
Date of Pregnancy Test
Item
If YES, Date of Test:
date
C0032976 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
If YES, Result:
integer
C0427777 (UMLS CUI [1])
Pregnancy Test Finding
Code List
If YES, Result:
CL Item
Negative (1)
CL Item
Positive (2)
Item Group
Completion of Dosing Period
C0805732 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Competion of maintenance period
Item
Did the patient complete the maintenance period?
boolean
C0805732 (UMLS CUI [1,1])
C0677908 (UMLS CUI [1,2])
Item
If the answer to the question is NO, check the one most significant reason below. Adverse Event
integer
C0877248 (UMLS CUI [1])
Adverse Event
Code List
If the answer to the question is NO, check the one most significant reason below. Adverse Event
CL Item
Adverse Event (1)
Adverse Event: Specification
Item
If the answer to the question is NO, check the one most significant reason below. Adverse event, specify:
text
C0877248 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
If the answer to the question is NO, check the one most significant reason below. Patient Request.
integer
C0332153 (UMLS CUI [1])
Patient Request
Code List
If the answer to the question is NO, check the one most significant reason below. Patient Request.
CL Item
Patient request (unrelated to AE) (2)
Patient Request: Specification
Item
If the answer to the question is NO, check the one most significant reason below. Patient request (unrelated to an AE), specify:
text
C0332153 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
If the answer to the question is NO, check the one most significant reason below. Non-compliance.
integer
C1321605 (UMLS CUI [1])
Compliance
Code List
If the answer to the question is NO, check the one most significant reason below. Non-compliance.
CL Item
Non-compliance (unrelated to an AE) (3)
Compliance: Specification
Item
If the answer to the question is NO, check the one most significant reason below. Non-compliance (unrelated to an AE), specify:
text
C1321605 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
If the answer to the question is NO, check the one most significant reason below. Investigator judgement.
integer
C0022423 (UMLS CUI [1])
Judgement
Code List
If the answer to the question is NO, check the one most significant reason below. Investigator judgement.
CL Item
Investigator judgement (4)
Judgement: Specification
Item
If the answer to the question is NO, check the one most significant reason below. Investigator judgement, specify:
text
C0022423 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
If the answer to the question is NO, check the one most significant reason below. Termination of patient dosing by sponsor.
integer
C0871548 (UMLS CUI [1])
Termination
Code List
If the answer to the question is NO, check the one most significant reason below. Termination of patient dosing by sponsor.
CL Item
Termination of patient dosing by sponsor (5)
Item
If the answer to the question is NO, check the one most significant reason below. Protocol Violation.
integer
C1709750 (UMLS CUI [1])
Protocol Violation
Code List
If the answer to the question is NO, check the one most significant reason below. Protocol Violation.
CL Item
Protocol violation (6)
Protocol Violation: Specification
Item
If the answer to the question is NO, check the one most significant reason below. Protocol violation, specify:
text
C1709750 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Item
If the answer to the question is NO, check the one most significant reason below. Death; complete the Patient Death CRF.
integer
C0011065 (UMLS CUI [1])
Death
Code List
If the answer to the question is NO, check the one most significant reason below. Death; complete the Patient Death CRF.
CL Item
Death; complete the Patient Death CRF (7)
Item
If the answer to the question is NO, check the one most significant reason below. Other.
integer
C3840932 (UMLS CUI [1])
Other Reason
Code List
If the answer to the question is NO, check the one most significant reason below. Other.
CL Item
Other (8)
Other Reason: Specification
Item
If the answer to the question is NO, check the one most significant reason below. Other, specify:
text
C3840932 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
End Date
Item
Date of study termination (last protocol assessment):
date
C0806020 (UMLS CUI [1])
Last Dosage
Item
Last dose in maintenance period:
float
C0178602 (UMLS CUI [1,1])
C1517741 (UMLS CUI [1,2])
Date of Last Dose
Item
Date of last dose in maintenance period:
date
C1762893 (UMLS CUI [1])
Down Titration
Item
Was the patient down-titrated for 1 week?
boolean
C2983683 (UMLS CUI [1,1])
C0205216 (UMLS CUI [1,2])
Down Titration: Reason
Item
Was the patient down-titrated for 1 week? If NO, please specify reason:
text
C2983683 (UMLS CUI [1,1])
C0205216 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
Down Titration: Duration
Item
Was the patient down-titrated for 1 week? If NO, specify duration of Down Titrationn:
text
C2983683 (UMLS CUI [1,1])
C0205216 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Down Titration: Last Dosage
Item
Last dose in Down-Titration:
float
C2983683 (UMLS CUI [1,1])
C0205216 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C1517741 (UMLS CUI [1,4])
Down Titration: Date of Last Dose
Item
Date of last Down-Titration Dose:
date
C2983683 (UMLS CUI [1,1])
C0205216 (UMLS CUI [1,2])
C1762893 (UMLS CUI [1,3])
Item Group
Investigator Signature
C2346576 (UMLS CUI-1)
Investigator's Signature
Item
To be completed by the Principal Investigator: I have assumed responsibility for completeness and accuracy of all data recorded on these Maintenance and Follow-Up Period Case Report Forms. Signature
text
C2346576 (UMLS CUI [1])
Investigator's Name
Item
To be completed by the Principal Investigator: I have assumed responsibility for completeness and accuracy of all data recorded on these Maintenance and Follow-Up Period Case Report Forms. Print Name:
text
C2826892 (UMLS CUI [1])
Date of Report
Item
Date
date
C1302584 (UMLS CUI [1])
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