ID

16267

Descrizione

Reducing Episodes by Septal Pacing Efficacy Confirmation Trial (RESPECT); ODM derived from: https://clinicaltrials.gov/show/NCT00289289

collegamento

https://clinicaltrials.gov/show/NCT00289289

Keywords

  1. 08/07/16 08/07/16 -
Caricato su

8 luglio 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT00289289

Eligibility Atrial Fibrillation NCT00289289

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects with fast and/or slow heartbeats who are in need of dual chamber pacing (pacing in both the atria and ventricles) as determined by their doctor.
Descrizione

need for dual chamber pacing

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2048107
UMLS CUI [1,2]
C0686904
subjects who have a history of occasional fast heartbeats originating from the upper heart chambers.
Descrizione

Supraventricular tachycardia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0039240
subjects who have experienced at least two symptomatic episodes of fast heartbeats three months prior to enrollment.
Descrizione

Supraventricular tachycardia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0039240
subjects that are expected to stay on the same heart medications during the length study.
Descrizione

heart medications

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2054143
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects who have permanent (chronic) or persistent (not self-terminating) atrial fibrillation (fast heartbeats originating from the upper heart chambers).
Descrizione

Chronic atrial fibrillation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0694539
subjects who have atrial fibrillation due to a reversible cause, i.e. electrolyte imbalance.
Descrizione

atrial fibrillation due to a reversible cause

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0205343
subjects who are current or immediate implantable cardioverter defibrillator (icd) recipients.
Descrizione

implantable cardioverter defibrillator

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0162589

Similar models

Eligibility Atrial Fibrillation NCT00289289

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
need for dual chamber pacing
Item
subjects with fast and/or slow heartbeats who are in need of dual chamber pacing (pacing in both the atria and ventricles) as determined by their doctor.
boolean
C2048107 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Supraventricular tachycardia
Item
subjects who have a history of occasional fast heartbeats originating from the upper heart chambers.
boolean
C0039240 (UMLS CUI [1])
Supraventricular tachycardia
Item
subjects who have experienced at least two symptomatic episodes of fast heartbeats three months prior to enrollment.
boolean
C0039240 (UMLS CUI [1])
heart medications
Item
subjects that are expected to stay on the same heart medications during the length study.
boolean
C2054143 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Chronic atrial fibrillation
Item
subjects who have permanent (chronic) or persistent (not self-terminating) atrial fibrillation (fast heartbeats originating from the upper heart chambers).
boolean
C0694539 (UMLS CUI [1])
atrial fibrillation due to a reversible cause
Item
subjects who have atrial fibrillation due to a reversible cause, i.e. electrolyte imbalance.
boolean
C0004238 (UMLS CUI [1,1])
C0205343 (UMLS CUI [1,2])
implantable cardioverter defibrillator
Item
subjects who are current or immediate implantable cardioverter defibrillator (icd) recipients.
boolean
C0162589 (UMLS CUI [1])

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