Informatie:
Fout:
ID
21451
Beschrijving
Endothelial Progenitor Cells and Nitric Oxide in Cardiac Rehabilitation Program Participants; ODM derived from: https://clinicaltrials.gov/show/NCT00308633
Link
https://clinicaltrials.gov/show/NCT00308633
Trefwoorden
Versies (1)
- 21-04-17 21-04-17 -
Geüploaded op
21 april 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Coronary Artery Disease (CAD) NCT00308633
Eligibility Coronary Artery Disease (CAD) NCT00308633
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Artery Disease (CAD) NCT00308633
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
age
Item
adults older than 21 years.
boolean
C0001779 (UMLS CUI [1])
coronary artery disease angiography
Item
coronary artery disease established by angiography.
boolean
C1956346 (UMLS CUI [1,1])
C0085532 (UMLS CUI [1,2])
C0085532 (UMLS CUI [1,2])
myocardial infarction, coronary artery bypass surgery interval
Item
at least two months interval since myocardial infarction or coronary artery bypass surgery.
boolean
C0027051 (UMLS CUI [1,1])
C1272706 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C1272706 (UMLS CUI [2,2])
C1272706 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C1272706 (UMLS CUI [2,2])
percutaneous coronary intervention, congestive heart failure symptoms interval
Item
at least one month interval since percutaneous coronary intervention or congestive heart failure symptoms.
boolean
C1532338 (UMLS CUI [1,1])
C1272706 (UMLS CUI [1,2])
C0018802 (UMLS CUI [2,1])
C1457887 (UMLS CUI [2,2])
C1272706 (UMLS CUI [2,3])
C1272706 (UMLS CUI [1,2])
C0018802 (UMLS CUI [2,1])
C1457887 (UMLS CUI [2,2])
C1272706 (UMLS CUI [2,3])
safe participation in cardiac rehabilitation
Item
no medical condition that might prohibit safe participation in cardiac rehabilitation.
boolean
C0700431 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,2])
informed consent
Item
subject understands protocol and provides written, informed consent in addition to willingness to comply with specified follow-up evaluations.
boolean
C0021430 (UMLS CUI [1])
structural heart disease by echocardiography
Item
significant structural heart disease (e.g. hypertrophic or dilated cardiomyopathy, valvular heart disease) as determined by echocardiography.
boolean
C1290384 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
C0013516 (UMLS CUI [1,2])
angina pectoris duration and response to nitroglycerin
Item
angina pectoris that is prolonged in duration (greater than 20 minutes), or does not respond to nitroglycerin (2 tablets) within 2 weeks of referral to the program.
boolean
C0002962 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0002962 (UMLS CUI [2,1])
C0017887 (UMLS CUI [2,2])
C0449238 (UMLS CUI [1,2])
C0002962 (UMLS CUI [2,1])
C0017887 (UMLS CUI [2,2])
cardiac rehabilitation ability
Item
subjects physically unable to perform cardiac rehabilitation protocol due to neurologic or orthopedic conditions.
boolean
C0700431 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,2])
pregnancy
Item
women of childbearing age unless recent pregnancy test is negative.
boolean
C0032961 (UMLS CUI [1])
breast feeding
Item
lactating women.
boolean
C0006147 (UMLS CUI [1])
implantable cardioverter defibrillator
Item
implantable cardioverter-defibrillator (icd)
boolean
C0162589 (UMLS CUI [1])