ID

33293

Beschrijving

Safety and Efficacy of Oral Versus Intravenous Amiodarone in the Treatment of AF; ODM derived from: https://clinicaltrials.gov/show/NCT01817439

Link

https://clinicaltrials.gov/show/NCT01817439

Trefwoorden

  1. 04-12-18 04-12-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

4 december 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01817439

Eligibility Atrial Fibrillation NCT01817439

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
over 18 years of age,
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients who will be admitted to the iccu / icu wards
Beschrijving

Patient Admission Intensive care unit

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030673
UMLS CUI [1,2]
C0021708
patients with recent onset of atrial fibrillation (duration < 48h).
Beschrijving

Atrial Fibrillation Onset Recent | Atrial Fibrillation Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0332162
UMLS CUI [1,3]
C0332185
UMLS CUI [2,1]
C0004238
UMLS CUI [2,2]
C0449238
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
baseline systolic blood pressure < 100 mm/hg
Beschrijving

Systolic Pressure

Datatype

boolean

Alias
UMLS CUI [1]
C0871470
known thyroid disease
Beschrijving

Thyroid Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0040128
serum potassium < 3.5 mmol/l
Beschrijving

Serum potassium measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0302353
pretreatment with amiodarone
Beschrijving

Pretreatment Amiodarone

Datatype

boolean

Alias
UMLS CUI [1,1]
C3539076
UMLS CUI [1,2]
C0002598
pregnant or lactating women.
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
participation in other clinical trial.
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Atrial Fibrillation NCT01817439

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
over 18 years of age,
boolean
C0001779 (UMLS CUI [1])
Patient Admission Intensive care unit
Item
patients who will be admitted to the iccu / icu wards
boolean
C0030673 (UMLS CUI [1,1])
C0021708 (UMLS CUI [1,2])
Atrial Fibrillation Onset Recent | Atrial Fibrillation Duration
Item
patients with recent onset of atrial fibrillation (duration < 48h).
boolean
C0004238 (UMLS CUI [1,1])
C0332162 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Age
Item
age < 18 years
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
baseline systolic blood pressure < 100 mm/hg
boolean
C0871470 (UMLS CUI [1])
Thyroid Disease
Item
known thyroid disease
boolean
C0040128 (UMLS CUI [1])
Serum potassium measurement
Item
serum potassium < 3.5 mmol/l
boolean
C0302353 (UMLS CUI [1])
Pretreatment Amiodarone
Item
pretreatment with amiodarone
boolean
C3539076 (UMLS CUI [1,1])
C0002598 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in other clinical trial.
boolean
C2348568 (UMLS CUI [1])

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