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Información:
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ID
15959
Descripción
Endothelial Dysfunction Evaluation for Coronary Heart Disease Risk Estimation in Rheumatoid Arthritis (EDRA Study); ODM derived from: https://clinicaltrials.gov/show/NCT02341066
Link
https://clinicaltrials.gov/show/NCT02341066
Palabras clave
Versiones (3)
- 21/6/16 21/6/16 -
- 21/6/16 21/6/16 -
- 24/6/16 24/6/16 -
Subido en
21 de junio de 2016
DOI
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Licencia
Creative Commons BY-NC 3.0
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Eligibility Rheumatoid Arthritis NCT02341066
Eligibility Rheumatoid Arthritis NCT02341066
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT02341066
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Rheumatoid Arthritis
Item
ra as defined by american college of rheumatology/european league against rheumatisms 2010 ra classification criteria
boolean
C0003873 (UMLS CUI [1])
Compliance behavior Study Protocol | Informed Consent
Item
in the opinion of investigators, patients must be able to adhere to the study visit schedule and must be capable of giving informed consent
boolean
C1321605 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
C2348563 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Cardiovascular event Previous | Event Cerebrovascular Previous | Acute Coronary Syndrome | Stable angina | Cerebrovascular accident | Interventional procedure | Carotid Endarterectomy | Peripheral arterial ischemia Symptomatic
Item
previous cardiovascular or cerebrovascular events (acute coronary syndrome, stable angina, stroke, interventional procedures, carotid endarterectomy, symptomatic peripheral artery ischemia)
boolean
C1320716 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0441471 (UMLS CUI [2,1])
C1880018 (UMLS CUI [2,2])
C0205156 (UMLS CUI [2,3])
C0948089 (UMLS CUI [3])
C0340288 (UMLS CUI [4])
C0038454 (UMLS CUI [5])
C0184661 (UMLS CUI [6])
C0014099 (UMLS CUI [7])
C3888991 (UMLS CUI [8,1])
C0231220 (UMLS CUI [8,2])
C0205156 (UMLS CUI [1,2])
C0441471 (UMLS CUI [2,1])
C1880018 (UMLS CUI [2,2])
C0205156 (UMLS CUI [2,3])
C0948089 (UMLS CUI [3])
C0340288 (UMLS CUI [4])
C0038454 (UMLS CUI [5])
C0184661 (UMLS CUI [6])
C0014099 (UMLS CUI [7])
C3888991 (UMLS CUI [8,1])
C0231220 (UMLS CUI [8,2])
Electrocardiogram abnormal At rest
Item
pathological ecg at rest
boolean
C0522055 (UMLS CUI [1,1])
C0443144 (UMLS CUI [1,2])
C0443144 (UMLS CUI [1,2])
Dysfunction of the autonomic nervous system Sign or Symptom
Item
sign or symptoms of autonomous nervous system dysfunction
boolean
C3277919 (UMLS CUI [1,1])
C3540840 (UMLS CUI [1,2])
C3540840 (UMLS CUI [1,2])
Communicable Diseases Serious
Item
serious infections in the previous 6 months
boolean
C0009450 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,2])
Comorbidity Severe | Hepatic Insufficiency | End stage renal disease | Glomerular Filtration Rate Cockcroft-Gault formula | cancer diagnosis Recent
Item
concomitant severe illness: overt hepatic insufficiency; end stage renal disease (glomerular filtration rate <30 ml/h at cockrofts-gault formula); recent diagnosis of cancer
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1306571 (UMLS CUI [2])
C0022661 (UMLS CUI [3])
C0017654 (UMLS CUI [4,1])
C2924627 (UMLS CUI [4,2])
C0920688 (UMLS CUI [5,1])
C0332185 (UMLS CUI [5,2])
C0205082 (UMLS CUI [1,2])
C1306571 (UMLS CUI [2])
C0022661 (UMLS CUI [3])
C0017654 (UMLS CUI [4,1])
C2924627 (UMLS CUI [4,2])
C0920688 (UMLS CUI [5,1])
C0332185 (UMLS CUI [5,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Relocation of home Planned | Clinical Study Site
Item
plans to leave target areas of each study site within three years
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C2347790 (UMLS CUI [2])
C1301732 (UMLS CUI [1,2])
C2347790 (UMLS CUI [2])