Informações:
Falhas:
ID
20440
Descrição
Effect of 6R-BH4 Treatment in Coronary Artery Disease (OXBIO Study); ODM derived from: https://clinicaltrials.gov/show/NCT00423280
Link
https://clinicaltrials.gov/show/NCT00423280
Palavras-chave
Versões (1)
- 22/02/2017 22/02/2017 -
Transferido a
22 de fevereiro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Coronary Artery Disease NCT00423280
Eligibility Coronary Artery Disease NCT00423280
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease NCT00423280
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Multi vessel coronary artery disease | Coronary Artery Bypass Surgery Scheduled
Item
multi-vessel coronary artery disease scheduled for coronary artery bypass surgery (cabg)
boolean
C1299432 (UMLS CUI [1])
C0010055 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C0010055 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Informed Consent Unable
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female subject who is pregnant, lactating or planning pregnancy during course of study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Heart failure Requirement Diuretic therapy | Left Ventricular Dysfunction Severe Evidence
Item
prior clinical diagnosis of heart failure requiring diuretic therapy with evidence of severe left ventricular dysfunction
boolean
C0018801 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0948575 (UMLS CUI [1,3])
C0242698 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C3887511 (UMLS CUI [2,3])
C1514873 (UMLS CUI [1,2])
C0948575 (UMLS CUI [1,3])
C0242698 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C3887511 (UMLS CUI [2,3])
Event Coronary
Item
recent acute coronary event (<4 weeks)
boolean
C0441471 (UMLS CUI [1,1])
C1522318 (UMLS CUI [1,2])
C1522318 (UMLS CUI [1,2])
Emergency CABG
Item
emergency cabg
boolean
C1532296 (UMLS CUI [1])
Diabetes Mellitus Newly Diagnosed
Item
newly diagnosed diabetes mellitus (<1 month)
boolean
C0011849 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C1518321 (UMLS CUI [1,2])
Body Weight
Item
body weight >130kg
boolean
C0005910 (UMLS CUI [1])
Renal Insufficiency | Creatinine measurement, serum
Item
impaired renal function (creatinine >180umol/l)
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0201976 (UMLS CUI [2])
Increased liver function tests | Alanine aminotransferase measurement | Aspartate aminotransferase increased
Item
elevated liver function tests (alt >50umol/l or ast >2x normal)
boolean
C0877359 (UMLS CUI [1])
C0201836 (UMLS CUI [2])
C0151904 (UMLS CUI [3])
C0201836 (UMLS CUI [2])
C0151904 (UMLS CUI [3])
Artificial cardiac pacemaker Consistent with Magnetic Resonance Imaging | Implantable defibrillator Consistent with Magnetic Resonance Imaging | Implants Metallic Consistent with Magnetic Resonance Imaging
Item
pacemakers, icds or metallic implants not compatible with mri scanning
boolean
C0030163 (UMLS CUI [1,1])
C0332290 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
C0162589 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0024485 (UMLS CUI [2,3])
C0021102 (UMLS CUI [3,1])
C2986473 (UMLS CUI [3,2])
C0332290 (UMLS CUI [3,3])
C0024485 (UMLS CUI [3,4])
C0332290 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
C0162589 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0024485 (UMLS CUI [2,3])
C0021102 (UMLS CUI [3,1])
C2986473 (UMLS CUI [3,2])
C0332290 (UMLS CUI [3,3])
C0024485 (UMLS CUI [3,4])
Investigational New Drugs | Study Subject Participation Status
Item
subjects receiving experimental medications or participating in another study
boolean
C0013230 (UMLS CUI [1])
C2348568 (UMLS CUI [2])
C2348568 (UMLS CUI [2])
Subject Terminally Ill
Item
terminally ill subjects
boolean
C0681850 (UMLS CUI [1,1])
C0039552 (UMLS CUI [1,2])
C0039552 (UMLS CUI [1,2])
Hypersensitivity Sapropterin
Item
known hypersensitivity to 6r-bh4
boolean
C0020517 (UMLS CUI [1,1])
C0048897 (UMLS CUI [1,2])
C0048897 (UMLS CUI [1,2])
Methotrexate | Levodopa | Phosphodiesterase 3 Inhibitors | Phosphodiesterase 5 inhibitor
Item
concomitant treatment with methotrexate, levodopa, pde-3 or pde-5 inhibitors
boolean
C0025677 (UMLS CUI [1])
C0023570 (UMLS CUI [2])
C2267032 (UMLS CUI [3])
C1318700 (UMLS CUI [4])
C0023570 (UMLS CUI [2])
C2267032 (UMLS CUI [3])
C1318700 (UMLS CUI [4])