ID

37526

Beschreibung

Intravenous Magnesium Infusion in Patients Undergoing Cardioversion of Atrial Fibrillation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01597557

Link

https://clinicaltrials.gov/show/NCT01597557

Stichworte

Versionen (1)
  1. 05.08.19 05.08.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

5. August 2019

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01597557

Englisch

Eligibility Atrial Fibrillation NCT01597557

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient with new onset atrial fibrillation less than 48 hours after onset undergoing electrical cardioversion.
Beschreibung

Atrial Fibrillation New onset | Status post Electric Countershock

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0746890
UMLS CUI [2,1]
C0231290
UMLS CUI [2,2]
C0013778
patients with atrial fibrillation longer than 48 hours on warfarin with documented therapeutic inr levels >2 for at least 3 weeks prior to the cardioversion, or been on dabigatran for 3 weeks, or a transesophageal echocardiogram on the day of the procedure that excludes intracardiac thrombi, undergoing electrical cardioversion.
Beschreibung

Atrial Fibrillation Disease length | Warfarin | International Normalized Ratio | Status pre- Electric Countershock | dabigatran | Transesophageal Echocardiography Excludes Thrombus of cardiac chamber

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0872146
UMLS CUI [2]
C0043031
UMLS CUI [3]
C0525032
UMLS CUI [4,1]
C0332152
UMLS CUI [4,2]
C0013778
UMLS CUI [5]
C2348066
UMLS CUI [6,1]
C0206054
UMLS CUI [6,2]
C0332196
UMLS CUI [6,3]
C0876998
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
creatinine >2.0 mg/dl
Beschreibung

Creatinine measurement, serum

Datentyp

boolean

Alias
UMLS CUI [1]
C0201976
potassium level less than 3.5 mmol/dl
Beschreibung

Potassium measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0202194
tsh < 0.5
Beschreibung

Thyroid stimulating hormone measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0202230
magnesium levels >3.0 mg/dl
Beschreibung

Magnesium measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0373675
urgent need for cardioversion (e.g., hemodynamic instability, unstable angina, pulmonary edema)
Beschreibung

Need Urgent Electric Countershock | Hemodynamic instability | Angina, Unstable | Pulmonary Edema

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027552
UMLS CUI [1,2]
C0439609
UMLS CUI [1,3]
C0013778
UMLS CUI [2]
C0948268
UMLS CUI [3]
C0002965
UMLS CUI [4]
C0034063
patients with recent (less than 6 weeks) acute myocardial infarction
Beschreibung

Myocardial Infarction Recent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0332185
patients post-cardiac surgery
Beschreibung

Status post Cardiac Surgery

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0231290
UMLS CUI [1,2]
C0018821
pregnant women
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
patients who are being treated with antiarrhythmic drugs who have received less than five doses of the drug. for amiodarone, patients who have received less than three weeks prior to cardioversion are excluded.
Beschreibung

Anti-Arrhythmia Agents Dose Quantity | Amiodarone

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003195
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1265611
UMLS CUI [2]
C0002598
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Ähnliche Modelle

Eligibility Atrial Fibrillation NCT01597557

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation New onset | Status post Electric Countershock
Item
patient with new onset atrial fibrillation less than 48 hours after onset undergoing electrical cardioversion.
boolean
C0004238 (UMLS CUI [1,1])
C0746890 (UMLS CUI [1,2])
C0231290 (UMLS CUI [2,1])
C0013778 (UMLS CUI [2,2])
Atrial Fibrillation Disease length | Warfarin | International Normalized Ratio | Status pre- Electric Countershock | dabigatran | Transesophageal Echocardiography Excludes Thrombus of cardiac chamber
Item
patients with atrial fibrillation longer than 48 hours on warfarin with documented therapeutic inr levels >2 for at least 3 weeks prior to the cardioversion, or been on dabigatran for 3 weeks, or a transesophageal echocardiogram on the day of the procedure that excludes intracardiac thrombi, undergoing electrical cardioversion.
boolean
C0004238 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0043031 (UMLS CUI [2])
C0525032 (UMLS CUI [3])
C0332152 (UMLS CUI [4,1])
C0013778 (UMLS CUI [4,2])
C2348066 (UMLS CUI [5])
C0206054 (UMLS CUI [6,1])
C0332196 (UMLS CUI [6,2])
C0876998 (UMLS CUI [6,3])
Item Group
C0680251 (UMLS CUI)
Creatinine measurement, serum
Item
creatinine >2.0 mg/dl
boolean
C0201976 (UMLS CUI [1])
Potassium measurement
Item
potassium level less than 3.5 mmol/dl
boolean
C0202194 (UMLS CUI [1])
Thyroid stimulating hormone measurement
Item
tsh < 0.5
boolean
C0202230 (UMLS CUI [1])
Magnesium measurement
Item
magnesium levels >3.0 mg/dl
boolean
C0373675 (UMLS CUI [1])
Need Urgent Electric Countershock | Hemodynamic instability | Angina, Unstable | Pulmonary Edema
Item
urgent need for cardioversion (e.g., hemodynamic instability, unstable angina, pulmonary edema)
boolean
C0027552 (UMLS CUI [1,1])
C0439609 (UMLS CUI [1,2])
C0013778 (UMLS CUI [1,3])
C0948268 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0034063 (UMLS CUI [4])
Myocardial Infarction Recent
Item
patients with recent (less than 6 weeks) acute myocardial infarction
boolean
C0027051 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
Status post Cardiac Surgery
Item
patients post-cardiac surgery
boolean
C0231290 (UMLS CUI [1,1])
C0018821 (UMLS CUI [1,2])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Anti-Arrhythmia Agents Dose Quantity | Amiodarone
Item
patients who are being treated with antiarrhythmic drugs who have received less than five doses of the drug. for amiodarone, patients who have received less than three weeks prior to cardioversion are excluded.
boolean
C0003195 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0002598 (UMLS CUI [2])
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