ID

22426

Descripción

Heart Rate Regularization in Patients With Permanent Atrial Fibrillation Post Marketing Study; ODM derived from: https://clinicaltrials.gov/show/NCT00246805

Link

https://clinicaltrials.gov/show/NCT00246805

Palabras clave

Versiones (1)
  1. 2/6/17 2/6/17 -
Subido en

2 de junio de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Permanent Atrial Fibrillation NCT00246805

Inglés

Eligibility Permanent Atrial Fibrillation NCT00246805

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient has signed informed consent form
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
patient with permanent atrial fibrillation, standard indication for vvi(r) pacing, and at least 1 episode of rate irregularity in the last month
Descripción

Permanent atrial fibrillation | Indication Pacemaker VVI | Indication Pacemaker VVIR | Irregular heart beat Episode of Quantity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2586056
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C0747134
UMLS CUI [3,1]
C3146298
UMLS CUI [3,2]
C0747139
UMLS CUI [4,1]
C0237314
UMLS CUI [4,2]
C0332189
UMLS CUI [4,3]
C1265611
new york heart association (nyha) class i, ii, iii
Descripción

New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1275491
patient is able to comply with follow-up times and will comply with the protocol
Descripción

Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0525058
> 18 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
paroxysmal atrial fibrillation
Descripción

Paroxysmal atrial fibrillation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0235480
nyha class iv
Descripción

New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1275491
left ventricular ejection fraction (lvef) < 35
Descripción

Left ventricular ejection fraction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428772
patients with unstable angina
Descripción

Angina, Unstable

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002965
patients who have experienced an acute myocardial infarction or received coronary artery revascularization (cabg), or coronary angioplasty (ptca) within 3 months prior to enrolment
Descripción

Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Transluminal Coronary Angioplasty

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0010055
UMLS CUI [3]
C2936173
patient candidate for cardiac surgery, or coronary angioplasty (ptca)
Descripción

Indication Cardiac Surgery procedures | Indication Percutaneous Transluminal Coronary Angioplasty

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0018821
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C2936173
patients who experienced a cardiovascular accident (cva) or transient ischemic attack (tia) with permanent disability
Descripción

Cerebrovascular accident | Transient Ischemic Attack | Permanent disability

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0007787
UMLS CUI [3]
C2135346
life expectancy < 12 months due to other medical conditions
Descripción

Life Expectancy Due to Other medical condition

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C3843040
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
the patient is enrolled in any concurrent (drug and/or device) study
Descripción

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
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Similar models

Eligibility Permanent Atrial Fibrillation NCT00246805

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
patient has signed informed consent form
boolean
C0021430 (UMLS CUI [1])
Permanent atrial fibrillation | Indication Pacemaker VVI | Indication Pacemaker VVIR | Irregular heart beat Episode of Quantity
Item
patient with permanent atrial fibrillation, standard indication for vvi(r) pacing, and at least 1 episode of rate irregularity in the last month
boolean
C2586056 (UMLS CUI [1])
C3146298 (UMLS CUI [2,1])
C0747134 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3,1])
C0747139 (UMLS CUI [3,2])
C0237314 (UMLS CUI [4,1])
C0332189 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
New York Heart Association Classification
Item
new york heart association (nyha) class i, ii, iii
boolean
C1275491 (UMLS CUI [1])
Protocol Compliance
Item
patient is able to comply with follow-up times and will comply with the protocol
boolean
C0525058 (UMLS CUI [1])
Age
Item
> 18 years of age
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Paroxysmal atrial fibrillation
Item
paroxysmal atrial fibrillation
boolean
C0235480 (UMLS CUI [1])
New York Heart Association Classification
Item
nyha class iv
boolean
C1275491 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction (lvef) < 35
boolean
C0428772 (UMLS CUI [1])
Angina, Unstable
Item
patients with unstable angina
boolean
C0002965 (UMLS CUI [1])
Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Transluminal Coronary Angioplasty
Item
patients who have experienced an acute myocardial infarction or received coronary artery revascularization (cabg), or coronary angioplasty (ptca) within 3 months prior to enrolment
boolean
C0027051 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
C2936173 (UMLS CUI [3])
Indication Cardiac Surgery procedures | Indication Percutaneous Transluminal Coronary Angioplasty
Item
patient candidate for cardiac surgery, or coronary angioplasty (ptca)
boolean
C3146298 (UMLS CUI [1,1])
C0018821 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C2936173 (UMLS CUI [2,2])
Cerebrovascular accident | Transient Ischemic Attack | Permanent disability
Item
patients who experienced a cardiovascular accident (cva) or transient ischemic attack (tia) with permanent disability
boolean
C0038454 (UMLS CUI [1])
C0007787 (UMLS CUI [2])
C2135346 (UMLS CUI [3])
Life Expectancy Due to Other medical condition
Item
life expectancy < 12 months due to other medical conditions
boolean
C0023671 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
the patient is enrolled in any concurrent (drug and/or device) study
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
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