Information:
Error:
Eligibility Heart Failure With Preserved Ejection Fraction NCT02078947
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Sedentary | Exercise Frequency mins/week
Item
sedentary (structured exercise < 2x 30 min/wk)
boolean
C0205254 (UMLS CUI [1])
C0015259 (UMLS CUI [2,1])
C0439603 (UMLS CUI [2,2])
C0556975 (UMLS CUI [2,3])
C0015259 (UMLS CUI [2,1])
C0439603 (UMLS CUI [2,2])
C0556975 (UMLS CUI [2,3])
Age
Item
at least 40 years old
boolean
C0001779 (UMLS CUI [1])
Function Systolic Maintained | Left ventricular ejection fraction
Item
preserved systolic function lvef > 50%
boolean
C0031843 (UMLS CUI [1,1])
C0039155 (UMLS CUI [1,2])
C1314677 (UMLS CUI [1,3])
C0428772 (UMLS CUI [2])
C0039155 (UMLS CUI [1,2])
C1314677 (UMLS CUI [1,3])
C0428772 (UMLS CUI [2])
Signs and Symptoms Heart failure New York Heart Association Classification
Item
signs and symptoms of heart failure class nyha ii or iii
boolean
C0037088 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0018801 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
Diastolic dysfunction | Other Coding | N-Terminal ProB-type Natriuretic Peptide Measurement
Item
diastolic dysfunction (e/é > 15 or e/é 8-15 and nt-probnp > 220 pg/ml)
boolean
C0520863 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
C3272900 (UMLS CUI [3])
C3846158 (UMLS CUI [2])
C3272900 (UMLS CUI [3])
Stable status Clinical
Item
clinically stable for >= 6 weeks
boolean
C0205360 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,2])
Therapy Optimal
Item
optimal medical treatment for >= 6 weeks
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
C2698651 (UMLS CUI [1,2])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Etiology aspects Heart failure Symptoms | Exception HFpEF | Valvular disease | Coronary Disease | Uncontrolled hypertension | Cardiac Arrhythmia Uncontrolled | Cardiomyopathy, Primary
Item
non- hfpef causes for hf symptoms (significant valvular or coronary disease, uncontrolled hypertension or arrhythmias, primary cardiomyopathies)
boolean
C0015127 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C4509226 (UMLS CUI [2,2])
C3258293 (UMLS CUI [3])
C1956346 (UMLS CUI [4])
C1868885 (UMLS CUI [5])
C0003811 (UMLS CUI [6,1])
C0205318 (UMLS CUI [6,2])
C0033141 (UMLS CUI [7])
C0018801 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C4509226 (UMLS CUI [2,2])
C3258293 (UMLS CUI [3])
C1956346 (UMLS CUI [4])
C1868885 (UMLS CUI [5])
C0003811 (UMLS CUI [6,1])
C0205318 (UMLS CUI [6,2])
C0033141 (UMLS CUI [7])
Lung disease | Percent predicted FEV1 | Chronic Obstructive Airway Disease Stage
Item
significant pulmonary disease (fev1 < 50% predicted, copd gold iii-iv)
boolean
C0024115 (UMLS CUI [1])
C0730561 (UMLS CUI [2])
C0024117 (UMLS CUI [3,1])
C1306673 (UMLS CUI [3,2])
C0730561 (UMLS CUI [2])
C0024117 (UMLS CUI [3,1])
C1306673 (UMLS CUI [3,2])
Exercise Unable | Condition Interferes with Exercise intervention
Item
inability to exercise or conditions that may interfere with exercise intervention
boolean
C0015259 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C1831738 (UMLS CUI [2,3])
C1299582 (UMLS CUI [1,2])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C1831738 (UMLS CUI [2,3])
Myocardial Infarction
Item
myocardial infarction in the previous three months
boolean
C0027051 (UMLS CUI [1])
Signs Ischemia | Exercise testing
Item
signs of ischemia during exercise testing
boolean
C0311392 (UMLS CUI [1,1])
C0022116 (UMLS CUI [1,2])
C0015260 (UMLS CUI [2])
C0022116 (UMLS CUI [1,2])
C0015260 (UMLS CUI [2])
Comorbidity Influence Prognosis
Item
comorbidity that may influence one- year prognosis
boolean
C0009488 (UMLS CUI [1,1])
C4054723 (UMLS CUI [1,2])
C0033325 (UMLS CUI [1,3])
C4054723 (UMLS CUI [1,2])
C0033325 (UMLS CUI [1,3])
Study Subject Participation Status
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])