ID

33293

Descripción

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

Palabras clave

  1. 4/12/18 4/12/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

4 de diciembre de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT01817439

Eligibility Atrial Fibrillation NCT01817439

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
over 18 years of age,
Descripción

Age

Tipo de datos

boolean

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

Patient Admission Intensive care unit

Tipo de datos

boolean

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

Atrial Fibrillation Onset Recent | Atrial Fibrillation Duration

Tipo de datos

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
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
age < 18 years
Descripción

Age

Tipo de datos

boolean

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

Systolic Pressure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0871470
known thyroid disease
Descripción

Thyroid Disease

Tipo de datos

boolean

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

Serum potassium measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0302353
pretreatment with amiodarone
Descripción

Pretreatment Amiodarone

Tipo de datos

boolean

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

Pregnancy | Breast Feeding

Tipo de datos

boolean

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

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Atrial Fibrillation NCT01817439

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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