ID

37544

Description

Genetically Determined Response to Atenolol in Patients With Persistent Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01719367

Link

https://clinicaltrials.gov/show/NCT01719367

Keywords

Versions (1)
  1. 8/6/19 8/6/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

August 6, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01719367

English

Eligibility Atrial Fibrillation NCT01719367

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects must be at least 18 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
subjects must have a history of persistent af currently treated with a rate control strategy.
Description

Persistent atrial fibrillation | Heart rate Control

Data type

boolean

Alias
UMLS CUI [1]
C2585653
UMLS CUI [2,1]
C0018810
UMLS CUI [2,2]
C2587213
subjects should be willing to give written, informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
subjects must be willing and able to participate in the exercise protocol.
Description

Participation Exercise Protocol

Data type

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0015259
UMLS CUI [1,3]
C2348563
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
new york heart association class iii or iv heart failure.
Description

Heart failure New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
a history of heart failure induced by tachy-arrhythmia.
Description

Heart failure Tachyarrhythmia Induced

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0080203
UMLS CUI [1,3]
C0205263
a history of coronary artery disease and the presence of at least one of the following:
Description

Coronary Artery Disease

Data type

boolean

Alias
UMLS CUI [1]
C1956346
canadian class iii or iv angina.
Description

Angina Pectoris Canadian Cardiovascular Society classification of angina

Data type

boolean

Alias
UMLS CUI [1,1]
C0002962
UMLS CUI [1,2]
C1277207
recent myocardial infarction, coronary artery bypass grafting, or percutaneous coronary intervention within 6 months.
Description

Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0010055
UMLS CUI [3]
C1532338
severe renal or hepatic impairment.
Description

Renal Insufficiency Severe | Hepatic impairment Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0948807
UMLS CUI [2,2]
C0205082
subjects who have a clinically significant allergy/intolerance to atenolol, including a history of beta-blocker induced bronchospasm.
Description

Atenolol allergy | Intolerance to Atenolol | Bronchial Spasm Adrenergic beta-Antagonist Induced

Data type

boolean

Alias
UMLS CUI [1]
C0570884
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0004147
UMLS CUI [3,1]
C0006266
UMLS CUI [3,2]
C0001645
UMLS CUI [3,3]
C0205263
females who are pregnant or nursing.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
history of severe av node dysfunction/pacemaker dependence.
Description

Atrioventricular node dysfunction Severe | Artificial cardiac pacemaker Dependence Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C3276314
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0030163
UMLS CUI [2,2]
C0439857
UMLS CUI [2,3]
C0205082
subjects who have a systolic blood pressure < 90 mm hg or resting vr <50 or >120 per minute on the day of the study.
Description

Systolic Pressure | Vascular resistance resting

Data type

boolean

Alias
UMLS CUI [1]
C0871470
UMLS CUI [2,1]
C0042380
UMLS CUI [2,2]
C0035253
patients currently taking vaughan-williams class i or iii anti-arrhythmic drugs.
Description

Anti-Arrhythmia Agents Class

Data type

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C0456387
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Similar models

Eligibility Atrial Fibrillation NCT01719367

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
subjects must be at least 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Persistent atrial fibrillation | Heart rate Control
Item
subjects must have a history of persistent af currently treated with a rate control strategy.
boolean
C2585653 (UMLS CUI [1])
C0018810 (UMLS CUI [2,1])
C2587213 (UMLS CUI [2,2])
Informed Consent
Item
subjects should be willing to give written, informed consent.
boolean
C0021430 (UMLS CUI [1])
Participation Exercise Protocol
Item
subjects must be willing and able to participate in the exercise protocol.
boolean
C0679823 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Heart failure New York Heart Association Classification
Item
new york heart association class iii or iv heart failure.
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Heart failure Tachyarrhythmia Induced
Item
a history of heart failure induced by tachy-arrhythmia.
boolean
C0018801 (UMLS CUI [1,1])
C0080203 (UMLS CUI [1,2])
C0205263 (UMLS CUI [1,3])
Coronary Artery Disease
Item
a history of coronary artery disease and the presence of at least one of the following:
boolean
C1956346 (UMLS CUI [1])
Angina Pectoris Canadian Cardiovascular Society classification of angina
Item
canadian class iii or iv angina.
boolean
C0002962 (UMLS CUI [1,1])
C1277207 (UMLS CUI [1,2])
Myocardial Infarction | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
recent myocardial infarction, coronary artery bypass grafting, or percutaneous coronary intervention within 6 months.
boolean
C0027051 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
Renal Insufficiency Severe | Hepatic impairment Severe
Item
severe renal or hepatic impairment.
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0948807 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Atenolol allergy | Intolerance to Atenolol | Bronchial Spasm Adrenergic beta-Antagonist Induced
Item
subjects who have a clinically significant allergy/intolerance to atenolol, including a history of beta-blocker induced bronchospasm.
boolean
C0570884 (UMLS CUI [1])
C1744706 (UMLS CUI [2,1])
C0004147 (UMLS CUI [2,2])
C0006266 (UMLS CUI [3,1])
C0001645 (UMLS CUI [3,2])
C0205263 (UMLS CUI [3,3])
Pregnancy | Breast Feeding
Item
females who are pregnant or nursing.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Atrioventricular node dysfunction Severe | Artificial cardiac pacemaker Dependence Severe
Item
history of severe av node dysfunction/pacemaker dependence.
boolean
C3276314 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0030163 (UMLS CUI [2,1])
C0439857 (UMLS CUI [2,2])
C0205082 (UMLS CUI [2,3])
Systolic Pressure | Vascular resistance resting
Item
subjects who have a systolic blood pressure < 90 mm hg or resting vr <50 or >120 per minute on the day of the study.
boolean
C0871470 (UMLS CUI [1])
C0042380 (UMLS CUI [2,1])
C0035253 (UMLS CUI [2,2])
Anti-Arrhythmia Agents Class
Item
patients currently taking vaughan-williams class i or iii anti-arrhythmic drugs.
boolean
C0003195 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
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