Informatie:
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ID
37477
Beschrijving
Effects of Intravenous K201 on the Restoration of Sinus Rhythm in Subjects With Symptomatic Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01259622
Link
https://clinicaltrials.gov/show/NCT01259622
Trefwoorden
Versies (1)
- 31-07-19 31-07-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
31 juli 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01259622
Eligibility Atrial Fibrillation NCT01259622
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01259622
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
ATRIAL FIBRILLATION SYMPTOMATIC Disease length
Item
symptomatic atrial fibrillation for more than 3 hours and less than 7 days (as dated by symptoms).
boolean
C0741283 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,2])
Atrial Fibrillation by ECG Finding
Item
atrial fibrillation documented by ecg at the start of study drug infusion.
boolean
C0344434 (UMLS CUI [1])
Exposure to K201
Item
previous exposure to k201
boolean
C0332157 (UMLS CUI [1,1])
C4534673 (UMLS CUI [1,2])
C4534673 (UMLS CUI [1,2])
QTcF - Fridericia's Correction Formula
Item
qtcf (fridericia correction) >440 ms
boolean
C1882513 (UMLS CUI [1])
QRS interval
Item
qrs interval > 140 ms
boolean
C0520880 (UMLS CUI [1])
Atrial-paced rhythm ECG | Ventricular-paced rhythm ECG
Item
paced atrial or paced ventricular rhythm on ecg
boolean
C1168320 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
C1168318 (UMLS CUI [2,1])
C0013798 (UMLS CUI [2,2])
C0013798 (UMLS CUI [1,2])
C1168318 (UMLS CUI [2,1])
C0013798 (UMLS CUI [2,2])
Administration of intravenous antiarrhythmic drug Class
Item
history of receiving another intravenous class i or class iii antiarrhythmic drug within 3 days of randomization
boolean
C4544567 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
C0456387 (UMLS CUI [1,2])
Amiodarone Oral | Amiodarone Intravenous
Item
history of amiodarone (oral or iv) in the last 3 months.
boolean
C0002598 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0002598 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
C1527415 (UMLS CUI [1,2])
C0002598 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
Acute Coronary Syndrome | Myocardial Infarction | Angina, Unstable
Item
clinical evidence or history of acute coronary syndrome (e.g. myocardial infarction, unstable angina) within 30 days prior to randomization
boolean
C0948089 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0027051 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
Electric Countershock failed
Item
history of failed electrical cardioversion at any time in the past
boolean
C0013778 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
Polymorphic ventricular tachycardia | Torsades de Pointes
Item
history of polymorphic ventricular tachycardia (e.g. torsades des pointes)
boolean
C0344432 (UMLS CUI [1])
C0040479 (UMLS CUI [2])
C0040479 (UMLS CUI [2])
Long QT Syndrome | Family history of long QT syndrome
Item
history or family history of long qt syndrome
boolean
C0023976 (UMLS CUI [1])
C3839836 (UMLS CUI [2])
C3839836 (UMLS CUI [2])
Ventricular Tachycardia Requirement Pharmacotherapy | Ventricular Tachycardia Requirement Device therapy
Item
history of ventricular tachycardia requiring drug or device therapy
boolean
C0042514 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,3])
C0042514 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C1504335 (UMLS CUI [2,3])
C1514873 (UMLS CUI [1,2])
C0013216 (UMLS CUI [1,3])
C0042514 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C1504335 (UMLS CUI [2,3])
Cardiac ejection fraction
Item
ejection fraction of 40% or less.
boolean
C0232174 (UMLS CUI [1])