ID

28399

Beschrijving

Sleep-Disordered Breathing in Heart Failure - The SchlaHF-Registry; ODM derived from: https://clinicaltrials.gov/show/NCT01500759

Link

https://clinicaltrials.gov/show/NCT01500759

Trefwoorden

Versies (1)
  1. 10-01-18 10-01-18 -
Houder van rechten

See clinicaltrials.gov

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10 januari 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Congestive Heart Failure NCT01500759

Engels

Eligibility Congestive Heart Failure NCT01500759

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must be over 18
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
chronic heart failure (at least 12 weeks since diagnosis) according to the current applicable guidelines
Beschrijving

Chronic heart failure Disease length

Datatype

boolean

Alias
UMLS CUI [1,1]
C0264716
UMLS CUI [1,2]
C0872146
left ventricular systolic dysfunction (lvef ≤ 45% by imaging method such as echocardiography, radionuclide angiography, left ventriculography, or cardiac magnetic resonance imaging) documented less than 12 weeks
Beschrijving

Left ventricular systolic dysfunction | Echocardiography: left ventricular ejection fraction | Left ventricular ejection fraction Radionuclide Angiography | Left ventricular ejection fraction Left ventriculography | Left ventricular ejection fraction Cardiac MRI

Datatype

boolean

Alias
UMLS CUI [1]
C1277187
UMLS CUI [2]
C2097013
UMLS CUI [3,1]
C0428772
UMLS CUI [3,2]
C0034604
UMLS CUI [4,1]
C0428772
UMLS CUI [4,2]
C0412219
UMLS CUI [5,1]
C0428772
UMLS CUI [5,2]
C0412692
nyha class iii or iv at the time of inclusion or nyha class ii with at least one hospitalisation for hf in the last 24 months
Beschrijving

Heart failure New York Heart Association Classification | Hospitalization Quantity Heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2,1]
C0019993
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0018801
patient is able to fully understand study information and signed informed consent
Beschrijving

Comprehension Study Protocol | Comprehension Informed Consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
life expectancy < 1 year for diseases unrelated to chronic hf
Beschrijving

Life Expectancy | Disease Independent of Chronic heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0332291
UMLS CUI [2,3]
C0264716
cardiac surgery, percutaneous coronary intervention (pci), myocardial infarction (mi) or unstable angina within 6 months
Beschrijving

Cardiac Surgery procedures | Percutaneous Coronary Intervention | Myocardial Infarction | Angina, Unstable

Datatype

boolean

Alias
UMLS CUI [1]
C0018821
UMLS CUI [2]
C1532338
UMLS CUI [3]
C0027051
UMLS CUI [4]
C0002965
crt-implantation (either crt-d or crt-p) scheduled or within 6 months
Beschrijving

Implantation of CRT-D Scheduled | CRT-P Implantation Scheduled | Implantation of CRT-D | CRT-P Implantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C1135480
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C1737639
UMLS CUI [2,2]
C0021107
UMLS CUI [2,3]
C0205539
UMLS CUI [3]
C1135480
UMLS CUI [4,1]
C1737639
UMLS CUI [4,2]
C0021107
transient ischemic attack (tia) or stroke within 3 months
Beschrijving

Transient Ischemic Attack | Cerebrovascular accident

Datatype

boolean

Alias
UMLS CUI [1]
C0007787
UMLS CUI [2]
C0038454
hemodynamically significant uncorrected primary valvular heart disease, obstructive or regurgitant, or any valvular disease expected to lead to surgery
Beschrijving

Primary valvular heart disease Obstructive | Primary valvular heart disease Regurgitation | Valvular disease Operative Surgical Procedures Expected

Datatype

boolean

Alias
UMLS CUI [1,1]
C2064629
UMLS CUI [1,2]
C0549186
UMLS CUI [2,1]
C2064629
UMLS CUI [2,2]
C2004489
UMLS CUI [3,1]
C3258293
UMLS CUI [3,2]
C0543467
UMLS CUI [3,3]
C1517001
acute myocarditis/pericarditis within 6 months
Beschrijving

Myocarditis | Pericarditis

Datatype

boolean

Alias
UMLS CUI [1]
C0027059
UMLS CUI [2]
C0031046
current cpap or bilevel therapy
Beschrijving

Continuous Positive Airway Pressure | Bilevel Continuous Positive Airway Pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0199451
UMLS CUI [2]
C1956423
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Similar models

Eligibility Congestive Heart Failure NCT01500759

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
patients must be over 18
boolean
C0001779 (UMLS CUI [1])
Chronic heart failure Disease length
Item
chronic heart failure (at least 12 weeks since diagnosis) according to the current applicable guidelines
boolean
C0264716 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Left ventricular systolic dysfunction | Echocardiography: left ventricular ejection fraction | Left ventricular ejection fraction Radionuclide Angiography | Left ventricular ejection fraction Left ventriculography | Left ventricular ejection fraction Cardiac MRI
Item
left ventricular systolic dysfunction (lvef ≤ 45% by imaging method such as echocardiography, radionuclide angiography, left ventriculography, or cardiac magnetic resonance imaging) documented less than 12 weeks
boolean
C1277187 (UMLS CUI [1])
C2097013 (UMLS CUI [2])
C0428772 (UMLS CUI [3,1])
C0034604 (UMLS CUI [3,2])
C0428772 (UMLS CUI [4,1])
C0412219 (UMLS CUI [4,2])
C0428772 (UMLS CUI [5,1])
C0412692 (UMLS CUI [5,2])
Heart failure New York Heart Association Classification | Hospitalization Quantity Heart failure
Item
nyha class iii or iv at the time of inclusion or nyha class ii with at least one hospitalisation for hf in the last 24 months
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C0019993 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0018801 (UMLS CUI [2,3])
Comprehension Study Protocol | Comprehension Informed Consent
Item
patient is able to fully understand study information and signed informed consent
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Life Expectancy | Disease Independent of Chronic heart failure
Item
life expectancy < 1 year for diseases unrelated to chronic hf
boolean
C0023671 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0332291 (UMLS CUI [2,2])
C0264716 (UMLS CUI [2,3])
Cardiac Surgery procedures | Percutaneous Coronary Intervention | Myocardial Infarction | Angina, Unstable
Item
cardiac surgery, percutaneous coronary intervention (pci), myocardial infarction (mi) or unstable angina within 6 months
boolean
C0018821 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
C0027051 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
Implantation of CRT-D Scheduled | CRT-P Implantation Scheduled | Implantation of CRT-D | CRT-P Implantation
Item
crt-implantation (either crt-d or crt-p) scheduled or within 6 months
boolean
C1135480 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C1737639 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
C0205539 (UMLS CUI [2,3])
C1135480 (UMLS CUI [3])
C1737639 (UMLS CUI [4,1])
C0021107 (UMLS CUI [4,2])
Transient Ischemic Attack | Cerebrovascular accident
Item
transient ischemic attack (tia) or stroke within 3 months
boolean
C0007787 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Primary valvular heart disease Obstructive | Primary valvular heart disease Regurgitation | Valvular disease Operative Surgical Procedures Expected
Item
hemodynamically significant uncorrected primary valvular heart disease, obstructive or regurgitant, or any valvular disease expected to lead to surgery
boolean
C2064629 (UMLS CUI [1,1])
C0549186 (UMLS CUI [1,2])
C2064629 (UMLS CUI [2,1])
C2004489 (UMLS CUI [2,2])
C3258293 (UMLS CUI [3,1])
C0543467 (UMLS CUI [3,2])
C1517001 (UMLS CUI [3,3])
Myocarditis | Pericarditis
Item
acute myocarditis/pericarditis within 6 months
boolean
C0027059 (UMLS CUI [1])
C0031046 (UMLS CUI [2])
Continuous Positive Airway Pressure | Bilevel Continuous Positive Airway Pressure
Item
current cpap or bilevel therapy
boolean
C0199451 (UMLS CUI [1])
C1956423 (UMLS CUI [2])
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