ID

34352

Description

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

Lien

https://clinicaltrials.gov/show/NCT00661323

Mots-clés

  1. 16/01/2019 16/01/2019 -
Détendeur de droits

GSK group of companies

Téléchargé le

16 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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Eligibility Ischemia NCT00661323

Eligibility Ischemia NCT00661323

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

Inclusion Criteria

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

ID.1

Type de données

boolean

adequate intravenous access in one arm
Description

ID.2

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

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

ID.3

Type de données

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
Description

ID.4

Type de données

boolean

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

ID.5

Type de données

boolean

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

ID.6

Type de données

boolean

abnormal ecg or chest pain syndrome
Description

ID.7

Type de données

boolean

claustrophobia
Description

ID.8

Type de données

boolean

resting heart rate greater than 110 bpm
Description

ID.9

Type de données

boolean

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

ID.10

Type de données

boolean

Similar models

Eligibility Ischemia NCT00661323

  1. StudyEvent: Eligibility
    1. Eligibility Ischemia NCT00661323
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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