ID

40489

Descripción

Copenhagen Study of Obese Patients With Ischemic Heart Disease Undergoing Low Energy Diet or Interval Training; ODM derived from: https://clinicaltrials.gov/show/NCT01724567

Link

https://clinicaltrials.gov/show/NCT01724567

Palabras clave

  1. 25/4/20 25/4/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

25 de abril de 2020

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT01724567

Eligibility Ischemic Heart Disease NCT01724567

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
stable ischemic heart disease
Descripción

Myocardial Ischemia Stable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0151744
UMLS CUI [1,2]
C0205360
bmi 28 - 40 kg/m2
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
known diabetes mellitus
Descripción

Diabetes Mellitus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
repeated fasting plasma glucose ≥ 7 mmol/l or hba1c > 7 %
Descripción

Plasma fasting glucose measurement | Hemoglobin A1c measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0583513
UMLS CUI [2]
C0474680
severe or moderate valve disease
Descripción

Valvular disease Severe | Valvular disease Moderate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3258293
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C3258293
UMLS CUI [2,2]
C0205081
main stem stenosis
Descripción

Coronary Artery Stenosis Main

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C1542147
severe heart failure, ejection fraction < 35 %
Descripción

Heart failure Severe | Cardiac ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0232174
physical or mental disability which are expected to prevent completion of intervention
Descripción

Physical disability Preventing Intervention | Mental handicap Preventing Intervention

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0520817
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C0184661
UMLS CUI [2,1]
C1306341
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C0184661
severe chronic obstructive pulmonary disease (copd) (fev1 < 50 % of expected) or asthma
Descripción

Severe chronic obstructive pulmonary disease | Percent predicted FEV1 | Asthma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0730607
UMLS CUI [2]
C0730561
UMLS CUI [3]
C0004096
active cancer
Descripción

Malignant Neoplasms

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
severe kidney (gfr < 40 ml/hour) or severe liver disease
Descripción

Kidney Disease Severe | Glomerular Filtration Rate | Liver disease Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0017654
UMLS CUI [3,1]
C0023895
UMLS CUI [3,2]
C0205082
severe ischemia or arrhythmias during exercise test
Descripción

Ischemia Severe During Exercise test | Cardiac Arrhythmia Severe During Exercise test

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0022116
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C0347984
UMLS CUI [1,4]
C0015260
UMLS CUI [2,1]
C0003811
UMLS CUI [2,2]
C0205082
UMLS CUI [2,3]
C0347984
UMLS CUI [2,4]
C0015260
2. or 3. degree atrio-ventricular (av) block, not protected by pacemaker
Descripción

Second degree atrioventricular block | Complete atrioventricular block | Artificial cardiac pacemaker Absent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0264906
UMLS CUI [2]
C0151517
UMLS CUI [3,1]
C0030163
UMLS CUI [3,2]
C0332197
organised training more than 2 times a week prior to inclusion
Descripción

Exercise times/week

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C0456698
significant weight loss or weight gain (> 5 %)3 month prior to inclusion
Descripción

Weight loss Percentage Timespan | Weight Gain Percentage Timespan

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1262477
UMLS CUI [1,2]
C0439165
UMLS CUI [1,3]
C0872291
UMLS CUI [2,1]
C0043094
UMLS CUI [2,2]
C0439165
UMLS CUI [2,3]
C0872291
not able to comprehend written and oral informed consent
Descripción

Informed Consent Comprehension Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
hormone treatment
Descripción

Hormone Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279025

Similar models

Eligibility Ischemic Heart Disease NCT01724567

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Myocardial Ischemia Stable
Item
stable ischemic heart disease
boolean
C0151744 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Body mass index
Item
bmi 28 - 40 kg/m2
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus
Item
known diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Plasma fasting glucose measurement | Hemoglobin A1c measurement
Item
repeated fasting plasma glucose ≥ 7 mmol/l or hba1c > 7 %
boolean
C0583513 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
Valvular disease Severe | Valvular disease Moderate
Item
severe or moderate valve disease
boolean
C3258293 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3258293 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
Coronary Artery Stenosis Main
Item
main stem stenosis
boolean
C0242231 (UMLS CUI [1,1])
C1542147 (UMLS CUI [1,2])
Heart failure Severe | Cardiac ejection fraction
Item
severe heart failure, ejection fraction < 35 %
boolean
C0018801 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0232174 (UMLS CUI [2])
Physical disability Preventing Intervention | Mental handicap Preventing Intervention
Item
physical or mental disability which are expected to prevent completion of intervention
boolean
C0520817 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C1306341 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])
Severe chronic obstructive pulmonary disease | Percent predicted FEV1 | Asthma
Item
severe chronic obstructive pulmonary disease (copd) (fev1 < 50 % of expected) or asthma
boolean
C0730607 (UMLS CUI [1])
C0730561 (UMLS CUI [2])
C0004096 (UMLS CUI [3])
Malignant Neoplasms
Item
active cancer
boolean
C0006826 (UMLS CUI [1])
Kidney Disease Severe | Glomerular Filtration Rate | Liver disease Severe
Item
severe kidney (gfr < 40 ml/hour) or severe liver disease
boolean
C0022658 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0017654 (UMLS CUI [2])
C0023895 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
Ischemia Severe During Exercise test | Cardiac Arrhythmia Severe During Exercise test
Item
severe ischemia or arrhythmias during exercise test
boolean
C0022116 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C0015260 (UMLS CUI [1,4])
C0003811 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,3])
C0015260 (UMLS CUI [2,4])
Second degree atrioventricular block | Complete atrioventricular block | Artificial cardiac pacemaker Absent
Item
2. or 3. degree atrio-ventricular (av) block, not protected by pacemaker
boolean
C0264906 (UMLS CUI [1])
C0151517 (UMLS CUI [2])
C0030163 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Exercise times/week
Item
organised training more than 2 times a week prior to inclusion
boolean
C0015259 (UMLS CUI [1,1])
C0456698 (UMLS CUI [1,2])
Weight loss Percentage Timespan | Weight Gain Percentage Timespan
Item
significant weight loss or weight gain (> 5 %)3 month prior to inclusion
boolean
C1262477 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])
C0043094 (UMLS CUI [2,1])
C0439165 (UMLS CUI [2,2])
C0872291 (UMLS CUI [2,3])
Informed Consent Comprehension Unable
Item
not able to comprehend written and oral informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Hormone Therapy
Item
hormone treatment
boolean
C0279025 (UMLS CUI [1])

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