Informações:
Falhas:
ID
37087
Descrição
Red Yeast Rice and Subclinical Atherosclerosis in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT02257047
Link
https://clinicaltrials.gov/show/NCT02257047
Palavras-chave
Versões (1)
- 02/07/2019 02/07/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
2 de julho de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT02257047
Eligibility Rheumatoid Arthritis NCT02257047
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT02257047
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Rheumatoid Arthritis | Classification Criteria Fulfill
Item
patients with a definite diagnose of rheumatoid arthritis(ra) were included if they met the classification criteria for ra established by the american rheumatism association (acr) and european league against rheumatism (eular) in 2010
boolean
C0003873 (UMLS CUI [1])
C0008902 (UMLS CUI [2,1])
C0243161 (UMLS CUI [2,2])
C1550543 (UMLS CUI [2,3])
C0008902 (UMLS CUI [2,1])
C0243161 (UMLS CUI [2,2])
C1550543 (UMLS CUI [2,3])
Age
Item
aged from 18 to 75 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent | Conflict Absent
Item
without conflict to the written, informed consent signed prior to the enrollment
boolean
C0021430 (UMLS CUI [1])
C0009671 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0009671 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Liver disease Severe Absent | Kidney Disease Severe Absent
Item
no severe hepatic or renal disorders
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0022658 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0205082 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0022658 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Carotid Stenosis Absent
Item
no known carotid artery stenosis
boolean
C0007282 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Blood Coagulation Disorder Absent
Item
no coagulation disorders
boolean
C0005779 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Hypertensive disease Absent
Item
no hypertension
boolean
C0020538 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
being in pregnancy, lactation period or under a pregnancy plan
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Hypersensitivity Investigational New Drugs
Item
being allergic to the test drug
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
Incompatibility Investigational New Drugs
Item
not compatible for the trial medication
boolean
C0679426 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
Legal capacity Limited
Item
without full legal capacity
boolean
C0683673 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,2])