ID

17170

Description

Open Label High Dose Ropinirole (Requip) Study for Patients With Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00260793

Link

https://clinicaltrials.gov/show/NCT00260793

Keywords

  1. 8/29/16 8/29/16 -
Uploaded on

August 29, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Parkinson's Disease NCT00260793

Eligibility Parkinson's Disease NCT00260793

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must give written informed consent prior to any specific study procedures.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
males or females; females of childbearing age who are not currently pregnant must agree to use a medically accepted method of contraception throughout the study.
Description

Contraception

Data type

boolean

Alias
UMLS CUI [1]
C0700589
age greater than or equal to 25 years.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients must be on a maximum dose of dopamine agonist drug (pergolide 4mg/day, pramipexole 4.5 mg/day or ropinirole 24mg/day).
Description

Maximum dose of dopamine agonist drug

Data type

boolean

Alias
UMLS CUI [1,1]
C0178601
UMLS CUI [1,2]
C0178602
stable dose of all medications for 4 weeks.
Description

Stable dose of all medications

Data type

boolean

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0205360
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
current hallucinations.
Description

Hallucinations

Data type

boolean

Alias
UMLS CUI [1]
C0018524
history of disabling hallucinations or hallucinations in past requiring treatment.
Description

Hallucinations requiring treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C0018524
UMLS CUI [1,2]
C0087111
troublesome edema (swelling).
Description

Edema

Data type

boolean

Alias
UMLS CUI [1]
C0013604
unstable depression.
Description

Depression

Data type

boolean

Alias
UMLS CUI [1]
C0011570
female who is pregnant or lactating.
Description

pregnant or lactating

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
use of an investigational drug with in the last 30 days.
Description

Investigational drug

Data type

boolean

Alias
UMLS CUI [1]
C0013230
other inclusion or exclusion criteria to be evaluated by the physician.
Description

Other inclusion or exclusion criteria

Data type

boolean

Alias
UMLS CUI [1]
C1516637

Similar models

Eligibility Parkinson's Disease NCT00260793

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
patients must give written informed consent prior to any specific study procedures.
boolean
C0021430 (UMLS CUI [1])
Contraception
Item
males or females; females of childbearing age who are not currently pregnant must agree to use a medically accepted method of contraception throughout the study.
boolean
C0700589 (UMLS CUI [1])
Age
Item
age greater than or equal to 25 years.
boolean
C0001779 (UMLS CUI [1])
Maximum dose of dopamine agonist drug
Item
patients must be on a maximum dose of dopamine agonist drug (pergolide 4mg/day, pramipexole 4.5 mg/day or ropinirole 24mg/day).
boolean
C0178601 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Stable dose of all medications
Item
stable dose of all medications for 4 weeks.
boolean
C0178602 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Hallucinations
Item
current hallucinations.
boolean
C0018524 (UMLS CUI [1])
Hallucinations requiring treatment
Item
history of disabling hallucinations or hallucinations in past requiring treatment.
boolean
C0018524 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Edema
Item
troublesome edema (swelling).
boolean
C0013604 (UMLS CUI [1])
Depression
Item
unstable depression.
boolean
C0011570 (UMLS CUI [1])
pregnant or lactating
Item
female who is pregnant or lactating.
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
Investigational drug
Item
use of an investigational drug with in the last 30 days.
boolean
C0013230 (UMLS CUI [1])
Other inclusion or exclusion criteria
Item
other inclusion or exclusion criteria to be evaluated by the physician.
boolean
C1516637 (UMLS CUI [1])

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