Informatie:
Fout:
ID
37566
Beschrijving
Potassium Infusion for Conversion of Atrial Fibrillation/-Flutter; ODM derived from: https://clinicaltrials.gov/show/NCT01818583
Link
https://clinicaltrials.gov/show/NCT01818583
Trefwoorden
Versies (1)
- 07-08-19 07-08-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
7 augustus 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01818583
Eligibility Atrial Fibrillation NCT01818583
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01818583
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])
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])
C0853028 (UMLS CUI [2])