Eligibility Atrial Fibrillation NCT01818583

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with paroxysmal atrial fibrillation/atrial flutter with duration <48 hours or <7 days and who are anticoagulated and have had inr >2 in >3 weeks
Descripción

Paroxysmal atrial fibrillation Duration | Paroxysmal atrial flutter Duration | Anticoagulation Therapy | International Normalized Ratio

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0235480
UMLS CUI [1,2]
C0449238
UMLS CUI [2,1]
C0741292
UMLS CUI [2,2]
C0449238
UMLS CUI [3]
C0003281
UMLS CUI [4]
C0525032
serum potassium ≤4,0 mmol/l.
Descripción

Serum potassium measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0302353
age ≥ 18 år
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
potassium > 4,0 mmol/l
Descripción

Potassium measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0202194
egfr <30 ml/min
Descripción

Estimated Glomerular Filtration Rate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3811844
patients on antiarrhythmic therapy (flecainid, amiodarone, dronedarone or sotalol)
Descripción

Anti-Arrhythmia Agents | Flecainide | Amiodarone | dronedarone | Sotalol

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003195
UMLS CUI [2]
C0016229
UMLS CUI [3]
C0002598
UMLS CUI [4]
C0766326
UMLS CUI [5]
C0037707
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
breast feeding
Descripción

Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
patients participating in a clinical trial during the last six months
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
addison disease, adynamia episodic hereditary, or sickle cell anemia
Descripción

Addison Disease | Adynamia episodica hereditaria | Anemia, Sickle Cell

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001403
UMLS CUI [2]
C0238357
UMLS CUI [3]
C0002895
metabolic acidosis, ph < 7,2
Descripción

Metabolic acidosis | Blood pH decreased

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0220981
UMLS CUI [2]
C0853028

Similar models

Eligibility Atrial Fibrillation NCT01818583

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Paroxysmal atrial fibrillation Duration | Paroxysmal atrial flutter Duration | Anticoagulation Therapy | International Normalized Ratio
Item
patients with paroxysmal atrial fibrillation/atrial flutter with duration <48 hours or <7 days and who are anticoagulated and have had inr >2 in >3 weeks
boolean
C0235480 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0741292 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0003281 (UMLS CUI [3])
C0525032 (UMLS CUI [4])
Serum potassium measurement
Item
serum potassium ≤4,0 mmol/l.
boolean
C0302353 (UMLS CUI [1])
Age
Item
age ≥ 18 år
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Potassium measurement
Item
potassium > 4,0 mmol/l
boolean
C0202194 (UMLS CUI [1])
Estimated Glomerular Filtration Rate
Item
egfr <30 ml/min
boolean
C3811844 (UMLS CUI [1])
Anti-Arrhythmia Agents | Flecainide | Amiodarone | dronedarone | Sotalol
Item
patients on antiarrhythmic therapy (flecainid, amiodarone, dronedarone or sotalol)
boolean
C0003195 (UMLS CUI [1])
C0016229 (UMLS CUI [2])
C0002598 (UMLS CUI [3])
C0766326 (UMLS CUI [4])
C0037707 (UMLS CUI [5])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
breast feeding
boolean
C0006147 (UMLS CUI [1])
Study Subject Participation Status
Item
patients participating in a clinical trial during the last six months
boolean
C2348568 (UMLS CUI [1])
Addison Disease | Adynamia episodica hereditaria | Anemia, Sickle Cell
Item
addison disease, adynamia episodic hereditary, or sickle cell anemia
boolean
C0001403 (UMLS CUI [1])
C0238357 (UMLS CUI [2])
C0002895 (UMLS CUI [3])
Metabolic acidosis | Blood pH decreased
Item
metabolic acidosis, ph < 7,2
boolean
C0220981 (UMLS CUI [1])
C0853028 (UMLS CUI [2])