Informations:
Erreur:
ID
16962
Description
Non Invasive Multicenter Italian Study for Coronary Artery Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00539604
Lien
https://clinicaltrials.gov/show/NCT00539604
Mots-clés
Versions (1)
- 16/08/2016 16/08/2016 -
Téléchargé le
16 août 2016
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Coronary Heart Disease NCT00539604
Eligibility Coronary Heart Disease NCT00539604
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Heart Disease NCT00539604
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Gender | Ethnic group Any | Coronary angiography Evaluation work up
Item
1. patients (men or women of any ethnic group) scheduled for a coronary angiography evaluation for a diagnostic work up.
boolean
C0079399 (UMLS CUI [1])
C0015031 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
C0085532 (UMLS CUI [3,1])
C0220825 (UMLS CUI [3,2])
C0750430 (UMLS CUI [3,3])
C0015031 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
C0085532 (UMLS CUI [3,1])
C0220825 (UMLS CUI [3,2])
C0750430 (UMLS CUI [3,3])
Coronary angiography | multidetector computed tomography Study
Item
2. patients will be expected to undergo coronary angiography within 2 weeks after the mdct study procedure. the coronary angiography must meet the minimum standard laid down in the protocol (see section 8.3.3).
boolean
C0085532 (UMLS CUI [1])
C2106966 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
C2106966 (UMLS CUI [2,1])
C2603343 (UMLS CUI [2,2])
Serum HDL cholesterol measurement | Serum total cholesterol measurement
Item
3. patients must have hdl and total cholesterol performed within the last year.
boolean
C0428472 (UMLS CUI [1])
C1445957 (UMLS CUI [2])
C1445957 (UMLS CUI [2])
Study Subject Participation Status | Protocol Compliance
Item
4. patients must be willing and able to continue study participation following the reference test to ensure completion of all procedures and observations required by the study.
boolean
C2348568 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
C0525058 (UMLS CUI [2])
Informed consent
Item
5. fully informed and signed consent must be obtained from each patient.
boolean
C0021430 (UMLS CUI [1])
Age
Item
1. patients under 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Investigational New Drug Received
Item
2. patients who have received any investigational drug within the 30 days prior to entering this study.
boolean
C0013230 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C1514756 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
3. pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Medical contraindication multidetector computed tomography Iodinated contrast media
Item
4. patients who have any contraindication to mdct examination with iodinate contrast media.
boolean
C1301624 (UMLS CUI [1,1])
C2106966 (UMLS CUI [1,2])
C1960405 (UMLS CUI [1,3])
C2106966 (UMLS CUI [1,2])
C1960405 (UMLS CUI [1,3])
heart rate | Adrenergic beta-Antagonists
Item
5. patients with heart rate >70 bpm despite of β-blocker treatment (see section 8.2.4.1).
boolean
C0018810 (UMLS CUI [1])
C0001645 (UMLS CUI [2])
C0001645 (UMLS CUI [2])
Sinus rhythm
Item
6. patients with no sinus rhythm.
boolean
C0232201 (UMLS CUI [1])
New York Heart Association Classification
Item
7. patients with nyha iii or iv class.
boolean
C1275491 (UMLS CUI [1])
Coronary Artery Bypass Surgery | Stenting
Item
8. patients who have previously undergone cabg or stenting.
boolean
C0010055 (UMLS CUI [1])
C2348535 (UMLS CUI [2])
C2348535 (UMLS CUI [2])
Creatinine measurement, serum
Item
9. patients with a creatinine value > 2 mg/dl.
boolean
C0201976 (UMLS CUI [1])