ID

17420

Beschrijving

Trip HF Study: Triple Resynchronization in Paced Heeart Failure Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00187265

Link

https://clinicaltrials.gov/show/NCT00187265

Trefwoorden

Versies (1)
  1. 13-09-16 13-09-16 -
Geüploaded op

13 september 2016

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Heart Failure NCT00187265

Engels

Eligibility Heart Failure NCT00187265

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
• nyha class iii–iv congestive heart failure, in spite of optimal medical treatment for their congestive heart failure for 1 month.
Beschrijving

Congestive heart failure Therapeutic procedure Optimal | New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C2698651
UMLS CUI [2]
C1275491
the medical treatment must include a 40 mg/day minimum dose of furosemide (or equivalent);
Beschrijving

Furosemide Daily Dose Minimum | Furosemide Equivalent Daily Dose Minimum

Datatype

boolean

Alias
UMLS CUI [1,1]
C0016860
UMLS CUI [1,2]
C2348070
UMLS CUI [1,3]
C1524031
UMLS CUI [2,1]
C0016860
UMLS CUI [2,2]
C0205163
UMLS CUI [2,3]
C2348070
UMLS CUI [2,4]
C1524031
permanent atrial fibrillation (af);
Beschrijving

Permanent atrial fibrillation

Datatype

boolean

Alias
UMLS CUI [1]
C2586056
left ventricular ejection fraction (lvef) ≤ 35%;
Beschrijving

Left ventricular ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0428772
indication for a pacemaker implantation for a permanent and symptomatic bradycardia, or already implanted pacemaker under the condition that leads positioning corresponds to the criteria described in the protocol;
Beschrijving

Indication Implantation of cardiac pacemaker | BRADYCARDIA SYMPTOMATIC Permanent | implanted pacemaker

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0189842
UMLS CUI [2,1]
C0741627
UMLS CUI [2,2]
C0205355
UMLS CUI [3]
C0848753
aortic pre-ejection delay at least equal to 140 ms.
Beschrijving

Pre ejection Delay Aortic

Datatype

boolean

Alias
UMLS CUI [1,1]
C2964374
UMLS CUI [1,2]
C0205421
UMLS CUI [1,3]
C0003483
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
indication for a cardiac defibrillator;
Beschrijving

Indication Defibrillator

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0180307
having presented a myocardial infarct within the previous 3 months;
Beschrijving

Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
having undergone cardiac surgery or coronary revascularization procedure within the previous 3 months, or being scheduled for such procedures;
Beschrijving

Cardiac Surgery procedures | Coronary revascularisation

Datatype

boolean

Alias
UMLS CUI [1]
C0018821
UMLS CUI [2]
C0877341
presenting chronic pulmonary insufficiency;
Beschrijving

Chronic pulmonary insufficiency

Datatype

boolean

Alias
UMLS CUI [1]
C3279625
patients whose congestive heart failure requires the use of an intravenous inotropic support;
Beschrijving

Congestive heart failure Requirement Inotropic agent Intravenous

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0304509
UMLS CUI [1,4]
C1522726
presenting a dysthyreosis;
Beschrijving

Thyroid dysfunction

Datatype

boolean

Alias
UMLS CUI [1]
C0348024
having a life expectancy of less than one year, for other reasons than the congestive heart failure;
Beschrijving

Life Expectancy | Congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
UMLS CUI [2]
C0018802
unable to be followed-up in the scope of the study for geographical reasons;
Beschrijving

Clinical Study Follow-up Adherence Unable Due to geographical area

Datatype

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1510802
UMLS CUI [1,3]
C1299582
UMLS CUI [1,4]
C0678226
UMLS CUI [1,5]
C0681784
having refused to give their consent;
Beschrijving

Informed Consent Refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116
minors (age < 18 years) and pregnant women.
Beschrijving

Minor | Age | Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0026193
UMLS CUI [2]
C0001779
UMLS CUI [3]
C0032961
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Similar models

Eligibility Heart Failure NCT00187265

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Congestive heart failure Therapeutic procedure Optimal | New York Heart Association Classification
Item
• nyha class iii–iv congestive heart failure, in spite of optimal medical treatment for their congestive heart failure for 1 month.
boolean
C0018802 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C2698651 (UMLS CUI [1,3])
C1275491 (UMLS CUI [2])
Furosemide Daily Dose Minimum | Furosemide Equivalent Daily Dose Minimum
Item
the medical treatment must include a 40 mg/day minimum dose of furosemide (or equivalent);
boolean
C0016860 (UMLS CUI [1,1])
C2348070 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,3])
C0016860 (UMLS CUI [2,1])
C0205163 (UMLS CUI [2,2])
C2348070 (UMLS CUI [2,3])
C1524031 (UMLS CUI [2,4])
Permanent atrial fibrillation
Item
permanent atrial fibrillation (af);
boolean
C2586056 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction (lvef) ≤ 35%;
boolean
C0428772 (UMLS CUI [1])
Indication Implantation of cardiac pacemaker | BRADYCARDIA SYMPTOMATIC Permanent | implanted pacemaker
Item
indication for a pacemaker implantation for a permanent and symptomatic bradycardia, or already implanted pacemaker under the condition that leads positioning corresponds to the criteria described in the protocol;
boolean
C3146298 (UMLS CUI [1,1])
C0189842 (UMLS CUI [1,2])
C0741627 (UMLS CUI [2,1])
C0205355 (UMLS CUI [2,2])
C0848753 (UMLS CUI [3])
Pre ejection Delay Aortic
Item
aortic pre-ejection delay at least equal to 140 ms.
boolean
C2964374 (UMLS CUI [1,1])
C0205421 (UMLS CUI [1,2])
C0003483 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Indication Defibrillator
Item
indication for a cardiac defibrillator;
boolean
C3146298 (UMLS CUI [1,1])
C0180307 (UMLS CUI [1,2])
Myocardial Infarction
Item
having presented a myocardial infarct within the previous 3 months;
boolean
C0027051 (UMLS CUI [1])
Cardiac Surgery procedures | Coronary revascularisation
Item
having undergone cardiac surgery or coronary revascularization procedure within the previous 3 months, or being scheduled for such procedures;
boolean
C0018821 (UMLS CUI [1])
C0877341 (UMLS CUI [2])
Chronic pulmonary insufficiency
Item
presenting chronic pulmonary insufficiency;
boolean
C3279625 (UMLS CUI [1])
Congestive heart failure Requirement Inotropic agent Intravenous
Item
patients whose congestive heart failure requires the use of an intravenous inotropic support;
boolean
C0018802 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0304509 (UMLS CUI [1,3])
C1522726 (UMLS CUI [1,4])
Thyroid dysfunction
Item
presenting a dysthyreosis;
boolean
C0348024 (UMLS CUI [1])
Life Expectancy | Congestive heart failure
Item
having a life expectancy of less than one year, for other reasons than the congestive heart failure;
boolean
C0023671 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
Clinical Study Follow-up Adherence Unable Due to geographical area
Item
unable to be followed-up in the scope of the study for geographical reasons;
boolean
C3274571 (UMLS CUI [1,1])
C1510802 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0678226 (UMLS CUI [1,4])
C0681784 (UMLS CUI [1,5])
Informed Consent Refused
Item
having refused to give their consent;
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Minor | Age | Pregnancy
Item
minors (age < 18 years) and pregnant women.
boolean
C0026193 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0032961 (UMLS CUI [3])
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