ID

13384

Description

Candesartan in the Prevention of Relapsing Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT00130975

Link

https://clinicaltrials.gov/show/NCT00130975

Keywords

Versions (1)
  1. 2/10/16 2/10/16 -
Uploaded on

February 10, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00130975

English

Eligibility Atrial Fibrillation NCT00130975

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Patients with atrial fibrillation, diagnosed electrocardiographically, of more than 48 hours duration in whom direct current (dc) cardioversion is planned.
Description

atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1]
C0004238
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
Patients with a history of known hypersensitivity or contraindication to any angiotensin ii receptor blocker or any angiotensin-converting enzyme (ace) inhibitor.
Description

hypersensitivit angiotensin ii receptor blocker or ACE inhibitor

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0521942
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0003015
Patients currently receiving an ace inhibitor or angiotensin ii antagonist because of heart failure or other strong indication.
Description

receiving medication because of heart failure

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0521942
UMLS CUI [1,4]
C0003015
Patients currently receiving any antiarrhythmic medication including sotalol. other beta-blockers will not be regarded as specific antiarrhythmic agents.
Description

antiarrhythmic medication

Data type

boolean

Alias
UMLS CUI [1]
C0003195
UMLS CUI [2]
C0037707
Significant renal artery stenosis and any medical condition in which administration of a vasodilator is contraindicated; serum creatinine > 225 micromol/l; or serum potassium > 5.5 mmol/l; or serum sodium < 128 mmol/l.
Description

renal artery stenosis

Data type

boolean

Alias
UMLS CUI [1]
C0035067
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0042402
UMLS CUI [3]
C0201976
UMLS CUI [4,1]
C0036743
UMLS CUI [4,2]
C0302353
UMLS CUI [5,1]
C0036743
UMLS CUI [5,2]
C0523891
UMLS CUI [6,1]
C0036743
UMLS CUI [6,2]
C0523891
Patients with severe hepatic dysfunction
Description

severe hepatic dysfunction

Data type

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205082
life-limiting disease or substance abuse which may affect participation.
Description

life-limiting disease or substance abuse

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0038586
Patients unwilling to participate
Description

unwilling to participate

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Patients who have previously undergone dc cardioversion for atrial fibrillation within the last month.
Description

dc cardioversion for atrial fibrillation

Data type

boolean

Alias
UMLS CUI [1,1]
C0542380
UMLS CUI [1,2]
C0004238
Thyrotoxicosis
Description

thyrotoxicosis

Data type

boolean

Alias
UMLS CUI [1]
C0040156
Patients with a systolic blood pressure of < 100 mm hg.
Description

systolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
Hypertensive patients requiring intensified treatment prior to dc cardioversion
Description

hypertensive patients

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2349975
UMLS CUI [1,3]
C0020538
Pregnancy or lactation
Description

pregnancy or lactation

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
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Similar models

Eligibility Atrial Fibrillation NCT00130975

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
atrial fibrillation
Item
Patients with atrial fibrillation, diagnosed electrocardiographically, of more than 48 hours duration in whom direct current (dc) cardioversion is planned.
boolean
C0004238 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hypersensitivit angiotensin ii receptor blocker or ACE inhibitor
Item
Patients with a history of known hypersensitivity or contraindication to any angiotensin ii receptor blocker or any angiotensin-converting enzyme (ace) inhibitor.
boolean
C0020517 (UMLS CUI [1,1])
C0521942 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0003015 (UMLS CUI [2,2])
receiving medication because of heart failure
Item
Patients currently receiving an ace inhibitor or angiotensin ii antagonist because of heart failure or other strong indication.
boolean
C0018801 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0521942 (UMLS CUI [1,3])
C0003015 (UMLS CUI [1,4])
antiarrhythmic medication
Item
Patients currently receiving any antiarrhythmic medication including sotalol. other beta-blockers will not be regarded as specific antiarrhythmic agents.
boolean
C0003195 (UMLS CUI [1])
C0037707 (UMLS CUI [2])
renal artery stenosis
Item
Significant renal artery stenosis and any medical condition in which administration of a vasodilator is contraindicated; serum creatinine > 225 micromol/l; or serum potassium > 5.5 mmol/l; or serum sodium < 128 mmol/l.
boolean
C0035067 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0042402 (UMLS CUI [2,3])
C0201976 (UMLS CUI [3])
C0036743 (UMLS CUI [4,1])
C0302353 (UMLS CUI [4,2])
C0036743 (UMLS CUI [5,1])
C0523891 (UMLS CUI [5,2])
C0036743 (UMLS CUI [6,1])
C0523891 (UMLS CUI [6,2])
severe hepatic dysfunction
Item
Patients with severe hepatic dysfunction
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
life-limiting disease or substance abuse
Item
life-limiting disease or substance abuse which may affect participation.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0038586 (UMLS CUI [2,3])
unwilling to participate
Item
Patients unwilling to participate
boolean
C0021430 (UMLS CUI [1])
dc cardioversion for atrial fibrillation
Item
Patients who have previously undergone dc cardioversion for atrial fibrillation within the last month.
boolean
C0542380 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
thyrotoxicosis
Item
Thyrotoxicosis
boolean
C0040156 (UMLS CUI [1])
systolic blood pressure
Item
Patients with a systolic blood pressure of < 100 mm hg.
boolean
C0871470 (UMLS CUI [1])
hypertensive patients
Item
Hypertensive patients requiring intensified treatment prior to dc cardioversion
boolean
C0087111 (UMLS CUI [1,1])
C2349975 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,3])
pregnancy or lactation
Item
Pregnancy or lactation
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
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