Eligibility Atrial Fibrillation NCT00225667

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
sinus node dysfunction (with or without av conduction disturbance)
Beskrivning

sinus node dysfunction

Datatyp

boolean

Alias
UMLS CUI [1]
C0428908
permanent, atrial or dual-chamber pacemaker implanted > 2 months before enrollment and with ability to record and store atrial high-rate episodes, frequency of mode switches and to perform non-invasive electrophysiologic testing
Beskrivning

permanent pacemaker

Datatyp

boolean

Alias
UMLS CUI [1]
C0281945
history of at least 6 ahre in the last 6 months (rate > 220/min, duration of > 2 minutes
Beskrivning

Atrial high rate episodes

Datatyp

boolean

Alias
UMLS CUI [1]
C0546959
history of prior diagnosis of hypertension and/or treated for hypertension or two documented bp > 130/85 (measurements done at least one week apart)
Beskrivning

Hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0020538
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
permanent or persistent af or more than 6 episodes of symptomatic paroxysmal af in the previous 6 months
Beskrivning

Atrial fibrillation

Datatyp

boolean

Alias
UMLS CUI [1]
C0004238
documented cr >200 umol/l and k+ >5.2 mmol/l in the previous 3 months
Beskrivning

Creatinine, Potassium

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C0202194
current treatment with a potassium sparing diuretic, unless serum potassium known to be in the normal range
Beskrivning

potassium sparing diuretic

Datatyp

boolean

Alias
UMLS CUI [1]
C0304490
lv ejection fraction known to be < 40 %
Beskrivning

LVEF

Datatyp

boolean

Alias
UMLS CUI [1]
C0428772
moderate or severe mitral regurgitation (3+, 4 +)
Beskrivning

mitral regurgitation

Datatyp

boolean

Alias
UMLS CUI [1]
C0026266
mitral stenosis of more than mild severity
Beskrivning

mitral stenosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0026269
aortic stenosis with mean gradient of > 25 mmhg
Beskrivning

aortic stenosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0003507
angina at rest in the last 2 months, or current ccs class 3 or 4 angina
Beskrivning

Unstable Angina, CCS class

Datatyp

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C1879987
unipolar atrial lead
Beskrivning

unipolar atrial lead

Datatyp

boolean

Alias
UMLS CUI [1]
C2016199
previous av node ablation
Beskrivning

av node ablation

Datatyp

boolean

Alias
UMLS CUI [1]
C3275044
p-wave amplitude less than 1.5 mv
Beskrivning

p-wave amplitude

Datatyp

boolean

Alias
UMLS CUI [1]
C3900074
current therapy with an ace inhibitor, arb or aldosterone antagonist
Beskrivning

ace inhibitor, arb or aldosterone antagonist

Datatyp

boolean

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C0521942
UMLS CUI [3]
C0002007
current or planned (within 6 months) with an anti-arrhythmic medication (amiodarone, sotalol, flecainide, propafenone, quinidine, dofetilide)
Beskrivning

anti-arrhythmic medication (amiodarone, sotalol, flecainide, propafenone, quinidine, dofetilide)

Datatyp

boolean

Alias
UMLS CUI [1]
C0002598
UMLS CUI [2]
C0037707
UMLS CUI [3]
C0016229
UMLS CUI [4]
C0033429
UMLS CUI [5]
C0034414
UMLS CUI [6]
C0114771

Similar models

Eligibility Atrial Fibrillation NCT00225667

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
sinus node dysfunction
Item
sinus node dysfunction (with or without av conduction disturbance)
boolean
C0428908 (UMLS CUI [1])
permanent pacemaker
Item
permanent, atrial or dual-chamber pacemaker implanted > 2 months before enrollment and with ability to record and store atrial high-rate episodes, frequency of mode switches and to perform non-invasive electrophysiologic testing
boolean
C0281945 (UMLS CUI [1])
Atrial high rate episodes
Item
history of at least 6 ahre in the last 6 months (rate > 220/min, duration of > 2 minutes
boolean
C0546959 (UMLS CUI [1])
Hypertension
Item
history of prior diagnosis of hypertension and/or treated for hypertension or two documented bp > 130/85 (measurements done at least one week apart)
boolean
C0020538 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Atrial fibrillation
Item
permanent or persistent af or more than 6 episodes of symptomatic paroxysmal af in the previous 6 months
boolean
C0004238 (UMLS CUI [1])
Creatinine, Potassium
Item
documented cr >200 umol/l and k+ >5.2 mmol/l in the previous 3 months
boolean
C0201976 (UMLS CUI [1])
C0202194 (UMLS CUI [2])
potassium sparing diuretic
Item
current treatment with a potassium sparing diuretic, unless serum potassium known to be in the normal range
boolean
C0304490 (UMLS CUI [1])
LVEF
Item
lv ejection fraction known to be < 40 %
boolean
C0428772 (UMLS CUI [1])
mitral regurgitation
Item
moderate or severe mitral regurgitation (3+, 4 +)
boolean
C0026266 (UMLS CUI [1])
mitral stenosis
Item
mitral stenosis of more than mild severity
boolean
C0026269 (UMLS CUI [1])
aortic stenosis
Item
aortic stenosis with mean gradient of > 25 mmhg
boolean
C0003507 (UMLS CUI [1])
Unstable Angina, CCS class
Item
angina at rest in the last 2 months, or current ccs class 3 or 4 angina
boolean
C0002965 (UMLS CUI [1])
C1879987 (UMLS CUI [2])
unipolar atrial lead
Item
unipolar atrial lead
boolean
C2016199 (UMLS CUI [1])
av node ablation
Item
previous av node ablation
boolean
C3275044 (UMLS CUI [1])
p-wave amplitude
Item
p-wave amplitude less than 1.5 mv
boolean
C3900074 (UMLS CUI [1])
ace inhibitor, arb or aldosterone antagonist
Item
current therapy with an ace inhibitor, arb or aldosterone antagonist
boolean
C0003015 (UMLS CUI [1])
C0521942 (UMLS CUI [2])
C0002007 (UMLS CUI [3])
anti-arrhythmic medication (amiodarone, sotalol, flecainide, propafenone, quinidine, dofetilide)
Item
current or planned (within 6 months) with an anti-arrhythmic medication (amiodarone, sotalol, flecainide, propafenone, quinidine, dofetilide)
boolean
C0002598 (UMLS CUI [1])
C0037707 (UMLS CUI [2])
C0016229 (UMLS CUI [3])
C0033429 (UMLS CUI [4])
C0034414 (UMLS CUI [5])
C0114771 (UMLS CUI [6])