Eligibility Heart Failure NCT01293526

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
must have been indicated for implantation or upgrade to a crt-d system in the last 3 months
Beskrivning

Indication Implantation of CRT-D

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1135480
indicated for crt according to current guidelines
Beskrivning

Indication CRT

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1167956
qrs duration between 120 ms and 150 ms
Beskrivning

QRS duration

Datatyp

boolean

Alias
UMLS CUI [1]
C0429025
able and willing to provide consent and authorization of use of phi
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
myocardial infarction or acute coronary syndrome deemed inappropriate for trial per the investigator within 90 days of implant
Beskrivning

Myocardial Infarction | Acute Coronary Syndrome

Datatyp

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0948089
planned, or recent heart surgery or revascularization within the last three months
Beskrivning

Cardiac Surgery Planned | Cardiac Surgery Recent | Revascularization Planned | Revascularization Recent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0018821
UMLS CUI [2,2]
C0332185
UMLS CUI [3,1]
C0581603
UMLS CUI [3,2]
C1301732
UMLS CUI [4,1]
C0581603
UMLS CUI [4,2]
C0332185
already enrolled in other study that precludes enrollment in this study per principal investigator
Beskrivning

Study Subject Participation Status | Clinical Trial

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
known pregnancy at the time of enrollment
Beskrivning

Pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
age less than 18 at the time of enrollment
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
unable to comply with follow-up requirements
Beskrivning

Compliance behavior Unable Follow-up

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C3274571
chronic atrial fibrillation
Beskrivning

Chronic atrial fibrillation

Datatyp

boolean

Alias
UMLS CUI [1]
C0694539
recent history of medical non-compliance as determined by the investigator
Beskrivning

Compliance behavior Lacking

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0332268
unable or unwilling to provide consent and authorization of use of phi
Beskrivning

Informed Consent Unable | Informed Consent Unwilling

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080

Similar models

Eligibility Heart Failure NCT01293526

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Indication Implantation of CRT-D
Item
must have been indicated for implantation or upgrade to a crt-d system in the last 3 months
boolean
C3146298 (UMLS CUI [1,1])
C1135480 (UMLS CUI [1,2])
Indication CRT
Item
indicated for crt according to current guidelines
boolean
C3146298 (UMLS CUI [1,1])
C1167956 (UMLS CUI [1,2])
QRS duration
Item
qrs duration between 120 ms and 150 ms
boolean
C0429025 (UMLS CUI [1])
Informed Consent
Item
able and willing to provide consent and authorization of use of phi
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Myocardial Infarction | Acute Coronary Syndrome
Item
myocardial infarction or acute coronary syndrome deemed inappropriate for trial per the investigator within 90 days of implant
boolean
C0027051 (UMLS CUI [1])
C0948089 (UMLS CUI [2])
Cardiac Surgery Planned | Cardiac Surgery Recent | Revascularization Planned | Revascularization Recent
Item
planned, or recent heart surgery or revascularization within the last three months
boolean
C0018821 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0018821 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
C0581603 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0581603 (UMLS CUI [4,1])
C0332185 (UMLS CUI [4,2])
Study Subject Participation Status | Clinical Trial
Item
already enrolled in other study that precludes enrollment in this study per principal investigator
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
Pregnancy
Item
known pregnancy at the time of enrollment
boolean
C0032961 (UMLS CUI [1])
Age
Item
age less than 18 at the time of enrollment
boolean
C0001779 (UMLS CUI [1])
Compliance behavior Unable Follow-up
Item
unable to comply with follow-up requirements
boolean
C1321605 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Chronic atrial fibrillation
Item
chronic atrial fibrillation
boolean
C0694539 (UMLS CUI [1])
Compliance behavior Lacking
Item
recent history of medical non-compliance as determined by the investigator
boolean
C1321605 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide consent and authorization of use of phi
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])