ID

12903

Description

The Atrial High Rate Episodes in Pacemaker Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00627328

Link

https://clinicaltrials.gov/show/NCT00627328

Keywords

  1. 1/5/16 1/5/16 -
Uploaded on

January 5, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Arrhythmia NCT00627328

Eligibility Arrhythmia NCT00627328

  1. StudyEvent: Eligibility
    1. Eligibility Arrhythmia NCT00627328
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing a medtronic kappa dr 700 or medtronic kappa 900 dr implant, for approved indications
Description

pacemaker

Data type

boolean

Alias
UMLS CUI [1]
C0030163
no previous history of pacemaker implantation
Description

pacemaker

Data type

boolean

Alias
UMLS CUI [1]
C0030163
patients 50 years of age or older
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with a history of atrial tachyarrhythmias (primary arm of study)
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
patients with medical conditions that would limit study participation
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
patients inaccessible for follow-up at the study center
Description

follow-up

Data type

boolean

Alias
UMLS CUI [1]
C1522577
patients incapable of providing informed consent
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patients with nyha classification of iv
Description

nyha

Data type

boolean

Alias
UMLS CUI [1]
C1275491
patients with a history of neurocardiogenic syncope, long qt syndrome, or hypertrophic obstructive cardiomyopathy (hocm)
Description

comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
patients taking sotalol or amiodorone
Description

sotalol, amiodarone

Data type

boolean

Alias
UMLS CUI [1]
C0037707
UMLS CUI [2]
C0002598
patients with a history of a prior icd or pacemaker implantation.
Description

icd, pacemaker

Data type

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C0030163

Similar models

Eligibility Arrhythmia NCT00627328

  1. StudyEvent: Eligibility
    1. Eligibility Arrhythmia NCT00627328
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
pacemaker
Item
patients undergoing a medtronic kappa dr 700 or medtronic kappa 900 dr implant, for approved indications
boolean
C0030163 (UMLS CUI [1])
pacemaker
Item
no previous history of pacemaker implantation
boolean
C0030163 (UMLS CUI [1])
age
Item
patients 50 years of age or older
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
comorbidity
Item
patients with a history of atrial tachyarrhythmias (primary arm of study)
boolean
C0009488 (UMLS CUI [1])
comorbidity
Item
patients with medical conditions that would limit study participation
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
follow-up
Item
patients inaccessible for follow-up at the study center
boolean
C1522577 (UMLS CUI [1])
informed consent
Item
patients incapable of providing informed consent
boolean
C0021430 (UMLS CUI [1])
nyha
Item
patients with nyha classification of iv
boolean
C1275491 (UMLS CUI [1])
comorbidity
Item
patients with a history of neurocardiogenic syncope, long qt syndrome, or hypertrophic obstructive cardiomyopathy (hocm)
boolean
C0009488 (UMLS CUI [1])
sotalol, amiodarone
Item
patients taking sotalol or amiodorone
boolean
C0037707 (UMLS CUI [1])
C0002598 (UMLS CUI [2])
icd, pacemaker
Item
patients with a history of a prior icd or pacemaker implantation.
boolean
C0162589 (UMLS CUI [1])
C0030163 (UMLS CUI [2])

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