Informações:
Falhas:
ID
17170
Descrição
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
Palavras-chave
Versões (1)
- 29/08/2016 29/08/2016 -
Transferido a
29 de agosto de 2016
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Parkinson's Disease NCT00260793
Eligibility Parkinson's Disease NCT00260793
- StudyEvent: Eligibility
Similar models
Eligibility Parkinson's Disease NCT00260793
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
C0205360 (UMLS CUI [1,2])
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])
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])
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])