ID

29472

Beschrijving

Triple Site Ventricular Stimulation for Cardiac Resynchronization Therapy (CRT) Candidates; ODM derived from: https://clinicaltrials.gov/show/NCT00887237

Link

https://clinicaltrials.gov/show/NCT00887237

Trefwoorden

Versies (1)
  1. 29-03-18 29-03-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

29 maart 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Heart Failure NCT00887237

Engels

Eligibility Heart Failure NCT00887237

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
> 18 years old
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
cardiac resynchronization indication : new york heart association (nyha) class iii/iv
Beschrijving

Indication Cardiac Resynchronization Therapy | New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1167956
UMLS CUI [2]
C1275491
& qrs width > 120 ms milliseconds (ms) or nyha class ii & qrs width > 150 ms
Beschrijving

QRS complex duration | New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1]
C0429025
UMLS CUI [2]
C1275491
sinus rhythm
Beschrijving

Sinus rhythm

Datatype

boolean

Alias
UMLS CUI [1]
C0232201
first implant procedure
Beschrijving

Implantation procedure First

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021107
UMLS CUI [1,2]
C0205435
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
permanent ventricular tachycardia
Beschrijving

Ventricular Tachycardia Permanent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0042514
UMLS CUI [1,2]
C0205355
permanent pacing indication for 3rd degree atrioventricular (av) block
Beschrijving

Indication Pacing Permanent | Complete atrioventricular block

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0199640
UMLS CUI [1,3]
C0205355
UMLS CUI [2]
C0151517
diagnosed or suspected acute myocarditis
Beschrijving

Myocarditis | Myocarditis Suspected

Datatype

boolean

Alias
UMLS CUI [1]
C0027059
UMLS CUI [2,1]
C0027059
UMLS CUI [2,2]
C0750491
less than 1 year life expectancy related to a non-cardiovascular disease
Beschrijving

Life Expectancy Due to Disease | Exception Cardiovascular Diseases

Datatype

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0012634
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007222
impossibility to perform follow-up in the investigative center
Beschrijving

Clinical Study Follow-up Perform Unsuccessful

Datatype

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0884358
UMLS CUI [1,3]
C1272705
pregnant woman
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
patient which may not cooperate to study procedures as evaluated by investigator
Beschrijving

Protocol Compliance Lacking

Datatype

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0332268
legally protected adult patient or patient unable to give an informed consent
Beschrijving

Protection of patient Legal | Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0412786
UMLS CUI [1,2]
C1301860
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
patient enrolled in an other clinical trial
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
patient which does not benefit from a social protection system
Beschrijving

Social Protection Benefit Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0242457
UMLS CUI [1,2]
C0814225
UMLS CUI [1,3]
C0332197
Renal Insufficiency
Beschrijving

Renal Insufficiency

Datatype

boolean

Alias
UMLS CUI [1]
C1565489
patient registered on a heart transplant waiting list
Beschrijving

Patient on waiting list Heart Transplantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0422768
UMLS CUI [1,2]
C0018823
disease and/or health condition which may interfere with study results
Beschrijving

Disease Interferes with Research results | Health condition Interferes with Research results

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0683954
UMLS CUI [2,1]
C2707304
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0683954
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Similar models

Eligibility Heart Failure NCT00887237

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
> 18 years old
boolean
C0001779 (UMLS CUI [1])
Indication Cardiac Resynchronization Therapy | New York Heart Association Classification
Item
cardiac resynchronization indication : new york heart association (nyha) class iii/iv
boolean
C3146298 (UMLS CUI [1,1])
C1167956 (UMLS CUI [1,2])
C1275491 (UMLS CUI [2])
QRS complex duration | New York Heart Association Classification
Item
& qrs width > 120 ms milliseconds (ms) or nyha class ii & qrs width > 150 ms
boolean
C0429025 (UMLS CUI [1])
C1275491 (UMLS CUI [2])
Sinus rhythm
Item
sinus rhythm
boolean
C0232201 (UMLS CUI [1])
Implantation procedure First
Item
first implant procedure
boolean
C0021107 (UMLS CUI [1,1])
C0205435 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Ventricular Tachycardia Permanent
Item
permanent ventricular tachycardia
boolean
C0042514 (UMLS CUI [1,1])
C0205355 (UMLS CUI [1,2])
Indication Pacing Permanent | Complete atrioventricular block
Item
permanent pacing indication for 3rd degree atrioventricular (av) block
boolean
C3146298 (UMLS CUI [1,1])
C0199640 (UMLS CUI [1,2])
C0205355 (UMLS CUI [1,3])
C0151517 (UMLS CUI [2])
Myocarditis | Myocarditis Suspected
Item
diagnosed or suspected acute myocarditis
boolean
C0027059 (UMLS CUI [1])
C0027059 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Life Expectancy Due to Disease | Exception Cardiovascular Diseases
Item
less than 1 year life expectancy related to a non-cardiovascular disease
boolean
C0023671 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0007222 (UMLS CUI [2,2])
Clinical Study Follow-up Perform Unsuccessful
Item
impossibility to perform follow-up in the investigative center
boolean
C3274571 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])
Pregnancy
Item
pregnant woman
boolean
C0032961 (UMLS CUI [1])
Protocol Compliance Lacking
Item
patient which may not cooperate to study procedures as evaluated by investigator
boolean
C0525058 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Protection of patient Legal | Informed Consent Unable
Item
legally protected adult patient or patient unable to give an informed consent
boolean
C0412786 (UMLS CUI [1,1])
C1301860 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Study Subject Participation Status
Item
patient enrolled in an other clinical trial
boolean
C2348568 (UMLS CUI [1])
Social Protection Benefit Absent
Item
patient which does not benefit from a social protection system
boolean
C0242457 (UMLS CUI [1,1])
C0814225 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Renal Insufficiency
Item
Renal Insufficiency
boolean
C1565489 (UMLS CUI [1])
Patient on waiting list Heart Transplantation
Item
patient registered on a heart transplant waiting list
boolean
C0422768 (UMLS CUI [1,1])
C0018823 (UMLS CUI [1,2])
Disease Interferes with Research results | Health condition Interferes with Research results
Item
disease and/or health condition which may interfere with study results
boolean
C0012634 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C2707304 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])
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