ID

19539

Description

Avoid FFS - Use of the Atrial Pacemaker Lead 1699 With Very Short Tip Ring Spacing to Avoid Far Field Sensing; ODM derived from: https://clinicaltrials.gov/show/NCT00512915

Link

https://clinicaltrials.gov/show/NCT00512915

Keywords

  1. 1/8/17 1/8/17 -
Uploaded on

January 8, 2017

DOI

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License

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT00512915

Eligibility Atrial Fibrillation NCT00512915

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
indication for dual chamber pacing
Description

Indication Cardiac pacing Dual Chamber

Data type

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0199640
UMLS CUI [1,3]
C0725893
implantation of an identity (adx) dr or victory or later pacemaker (st. jude medical)
Description

Implantation of cardiac pacemaker

Data type

boolean

Alias
UMLS CUI [1]
C0189842
bipolar atrial pacing electrode
Description

Atrial pacing Electrode Bipolar

Data type

boolean

Alias
UMLS CUI [1,1]
C0199647
UMLS CUI [1,2]
C0013812
UMLS CUI [1,3]
C0443156
age >= 18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
persistent / permanent atrial arrhythmia
Description

Atrial arrhythmia persistent | Atrial arrhythmia Permanent

Data type

boolean

Alias
UMLS CUI [1,1]
C0085611
UMLS CUI [1,2]
C0205322
UMLS CUI [2,1]
C0085611
UMLS CUI [2,2]
C0205355
pacemaker revision
Description

Repair of cardiac pacemaker

Data type

boolean

Alias
UMLS CUI [1]
C0189860
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
participation in another study involving active implantable medical devices
Description

Study Subject Participation Status | Implant, device

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0021102
unable to complete follow up
Description

Follow-up Complete Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C1299582
missing patient informed consent
Description

Informed Consent Missing

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705492
cardiac surgery or myocardial infarction within the last 4 weeks
Description

Cardiac Surgery | Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1]
C0018821
UMLS CUI [2]
C0027051
planned cardiac surgery within 3 months after enrollment
Description

Cardiac Surgery Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0018821
UMLS CUI [1,2]
C1301732

Similar models

Eligibility Atrial Fibrillation NCT00512915

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Indication Cardiac pacing Dual Chamber
Item
indication for dual chamber pacing
boolean
C3146298 (UMLS CUI [1,1])
C0199640 (UMLS CUI [1,2])
C0725893 (UMLS CUI [1,3])
Implantation of cardiac pacemaker
Item
implantation of an identity (adx) dr or victory or later pacemaker (st. jude medical)
boolean
C0189842 (UMLS CUI [1])
Atrial pacing Electrode Bipolar
Item
bipolar atrial pacing electrode
boolean
C0199647 (UMLS CUI [1,1])
C0013812 (UMLS CUI [1,2])
C0443156 (UMLS CUI [1,3])
Age
Item
age >= 18 years
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Atrial arrhythmia persistent | Atrial arrhythmia Permanent
Item
persistent / permanent atrial arrhythmia
boolean
C0085611 (UMLS CUI [1,1])
C0205322 (UMLS CUI [1,2])
C0085611 (UMLS CUI [2,1])
C0205355 (UMLS CUI [2,2])
Repair of cardiac pacemaker
Item
pacemaker revision
boolean
C0189860 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status | Implant, device
Item
participation in another study involving active implantable medical devices
boolean
C2348568 (UMLS CUI [1])
C0021102 (UMLS CUI [2])
Follow-up Complete Unable
Item
unable to complete follow up
boolean
C3274571 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Informed Consent Missing
Item
missing patient informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1705492 (UMLS CUI [1,2])
Cardiac Surgery | Myocardial Infarction
Item
cardiac surgery or myocardial infarction within the last 4 weeks
boolean
C0018821 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
Cardiac Surgery Planned
Item
planned cardiac surgery within 3 months after enrollment
boolean
C0018821 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])

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