ID

34352

Descripción

Evaluating a New Echocardiography Imaging Procedure for Evaluating Heart Function; ODM derived from: https://clinicaltrials.gov/show/NCT00661323

Link

https://clinicaltrials.gov/show/NCT00661323

Palabras clave

  1. 16/1/19 16/1/19 -
Titular de derechos de autor

GSK group of companies

Subido en

16 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Ischemia NCT00661323

Eligibility Ischemia NCT00661323

  1. StudyEvent: Eligibility
    1. Eligibility Ischemia NCT00661323
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
no evidence of underlying cardiac disease based on history or electrocardiogram (ecg)
Descripción

ID.1

Tipo de datos

boolean

adequate intravenous access in one arm
Descripción

ID.2

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breastfeeding; if pre-menopausal, not practicing acceptable method of birth control
Descripción

ID.3

Tipo de datos

boolean

history of any other medical condition that is likely to hinder study conduct or pose a safety concern, in the opinion of the investigator
Descripción

ID.4

Tipo de datos

boolean

history of cardiac disease, including heart attack or heart valve disease
Descripción

ID.5

Tipo de datos

boolean

uncontrolled high blood pressure, defined as systolic blood pressure higher than 160 mm hg and/or diastolic pressure higher than 100 mm hg
Descripción

ID.6

Tipo de datos

boolean

abnormal ecg or chest pain syndrome
Descripción

ID.7

Tipo de datos

boolean

claustrophobia
Descripción

ID.8

Tipo de datos

boolean

resting heart rate greater than 110 bpm
Descripción

ID.9

Tipo de datos

boolean

unable to undergo mri procedure (e.g., pacemaker, metallic implants)
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Ischemia NCT00661323

  1. StudyEvent: Eligibility
    1. Eligibility Ischemia NCT00661323
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
no evidence of underlying cardiac disease based on history or electrocardiogram (ecg)
boolean
ID.2
Item
adequate intravenous access in one arm
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
pregnant or breastfeeding; if pre-menopausal, not practicing acceptable method of birth control
boolean
ID.4
Item
history of any other medical condition that is likely to hinder study conduct or pose a safety concern, in the opinion of the investigator
boolean
ID.5
Item
history of cardiac disease, including heart attack or heart valve disease
boolean
ID.6
Item
uncontrolled high blood pressure, defined as systolic blood pressure higher than 160 mm hg and/or diastolic pressure higher than 100 mm hg
boolean
ID.7
Item
abnormal ecg or chest pain syndrome
boolean
ID.8
Item
claustrophobia
boolean
ID.9
Item
resting heart rate greater than 110 bpm
boolean
ID.10
Item
unable to undergo mri procedure (e.g., pacemaker, metallic implants)
boolean

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