ID

22426

Description

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

Keywords

Versions (1)
  1. 6/2/17 6/2/17 -
Uploaded on

June 2, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Permanent Atrial Fibrillation NCT00246805

English

Eligibility Permanent Atrial Fibrillation NCT00246805

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient has signed informed consent form
Description

Informed Consent

Data type

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
Description

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

Data type

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
Description

New York Heart Association Classification

Data type

boolean

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

Protocol Compliance

Data type

boolean

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

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
paroxysmal atrial fibrillation
Description

Paroxysmal atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C0235480
nyha class iv
Description

New York Heart Association Classification

Data type

boolean

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

Left ventricular ejection fraction

Data type

boolean

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

Angina, Unstable

Data type

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
Description

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

Data type

boolean

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

Indication Cardiac Surgery procedures | Indication Percutaneous Transluminal Coronary Angioplasty

Data type

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
Description

Cerebrovascular accident | Transient Ischemic Attack | Permanent disability

Data type

boolean

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

Life Expectancy Due to Other medical condition

Data type

boolean

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

Pregnancy

Data type

boolean

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

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

Data type

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 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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