ID

19539

Descripción

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

Palabras clave

Versiones (1)
  1. 8/1/17 8/1/17 -
Subido en

8 de enero de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00512915

Inglés

Eligibility Atrial Fibrillation NCT00512915

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
indication for dual chamber pacing
Descripción

Indication Cardiac pacing Dual Chamber

Tipo de datos

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)
Descripción

Implantation of cardiac pacemaker

Tipo de datos

boolean

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

Atrial pacing Electrode Bipolar

Tipo de datos

boolean

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

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
persistent / permanent atrial arrhythmia
Descripción

Atrial arrhythmia persistent | Atrial arrhythmia Permanent

Tipo de datos

boolean

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

Repair of cardiac pacemaker

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0189860
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

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

Study Subject Participation Status | Implant, device

Tipo de datos

boolean

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

Follow-up Complete Unable

Tipo de datos

boolean

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

Informed Consent Missing

Tipo de datos

boolean

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

Cardiac Surgery | Myocardial Infarction

Tipo de datos

boolean

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

Cardiac Surgery Planned

Tipo de datos

boolean

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

Eligibility Atrial Fibrillation NCT00512915

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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