Informações:
Falhas:
ID
31439
Descrição
The Parkinson's Disease NeuroGenebank at Scripps Clinic Registry; ODM derived from: https://clinicaltrials.gov/show/NCT00766948
Link
https://clinicaltrials.gov/show/NCT00766948
Palavras-chave
Versões (1)
- 21/08/2018 21/08/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
21 de agosto de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Parkinson's Disease NCT00766948
Eligibility Parkinson's Disease NCT00766948
- StudyEvent: Eligibility
Similar models
Eligibility Parkinson's Disease NCT00766948
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Age
Item
is age 30 years or older at the time of onset of parkinson's
boolean
C0001779 (UMLS CUI [1])
Parkinson Disease
Item
has been diagnosed with idiopathic parkinson's disease by a scripps neurologist
boolean
C0030567 (UMLS CUI [1])
Protocol Compliance | Protocol Compliance Patient Representatives | Protocol Compliance Legal Guardians
Item
is reliable, cooperative and willing to comply with all protocol-specified procedures and/or sub-study if consented or have legal representative/guardian willing to do so
boolean
C0525058 (UMLS CUI [1])
C0525058 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3,1])
C0023226 (UMLS CUI [3,2])
C0525058 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
C0525058 (UMLS CUI [3,1])
C0023226 (UMLS CUI [3,2])
Informed Consent | Informed Consent Patient Representatives
Item
able to understand and grant informed consent or have a legal representative/
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Informed Consent Legal Guardians
Item
guardian who is able to do so
boolean
C0021430 (UMLS CUI [1,1])
C0023226 (UMLS CUI [1,2])
C0023226 (UMLS CUI [1,2])
Study Subject Participation Status
Item
patient has been previously enrolled in the parkinson's disease neurogenebank at scripps clinic registry
boolean
C2348568 (UMLS CUI [1])
Medical contraindication Blood draw
Item
if a blood draw would be contraindicated for any reason
boolean
C1301624 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,2])
Medical condition chronic Interferes with Study Subject Participation Status | Cerebrovascular accident | Hepatic Encephalopathy
Item
has a significant chronic medical condition (i.e. cva, hepatic encephalopathy) which, in the investigator's option, may interfere with the patient's optimal participation in the study
boolean
C3843040 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0521102 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,4])
C0038454 (UMLS CUI [2])
C0019151 (UMLS CUI [3])
C0205191 (UMLS CUI [1,2])
C0521102 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,4])
C0038454 (UMLS CUI [2])
C0019151 (UMLS CUI [3])
Investigational New Drugs | Investigational Medical Device
Item
treatment with any investigational agents or devices within 30 days preceding enrollment in the study
boolean
C0013230 (UMLS CUI [1])
C2346570 (UMLS CUI [2])
C2346570 (UMLS CUI [2])
Electroconvulsive Therapy
Item
has undergone ect within 90 days preceding enrollment in the study
boolean
C0013806 (UMLS CUI [1])