ID

40480

Descripción

Detecting Heart Disease Using First Pass Imaging With Gated SPECT Perfusion; ODM derived from: https://clinicaltrials.gov/show/NCT01137409

Link

https://clinicaltrials.gov/show/NCT01137409

Palabras clave

  1. 25/4/20 25/4/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

25 de abril de 2020

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT01137409

Eligibility Ischemic Heart Disease NCT01137409

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females age 18 through 80 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
female patients who are: surgically sterile (hysterectomy or bilateral tubule libation), at least one year post-menopausal, or have a negative pregnancy test on the day of treatment
Descripción

Gender | Female Sterilization | Hysterectomy | Bilateral tubal ligation | Postmenopausal state Duration | Pregnancy test negative

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0015787
UMLS CUI [3]
C0020699
UMLS CUI [4]
C0589114
UMLS CUI [5,1]
C0232970
UMLS CUI [5,2]
C0449238
UMLS CUI [6]
C0427780
written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient consumed food/beverage/medication containing caffeine/methylxanthines up to 12 hours prior to infusion
Descripción

Food Containing Caffeine | Beverages Containing Caffeine | Pharmaceutical Preparations Containing Caffeine | Food Containing Methylxanthine | Beverages Containing Methylxanthine | Pharmaceutical Preparations Containing Methylxanthine

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0016452
UMLS CUI [1,2]
C0332256
UMLS CUI [1,3]
C0006644
UMLS CUI [2,1]
C0005329
UMLS CUI [2,2]
C0332256
UMLS CUI [2,3]
C0006644
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C0332256
UMLS CUI [3,3]
C0006644
UMLS CUI [4,1]
C0016452
UMLS CUI [4,2]
C0332256
UMLS CUI [4,3]
C0066447
UMLS CUI [5,1]
C0005329
UMLS CUI [5,2]
C0332256
UMLS CUI [5,3]
C0066447
UMLS CUI [6,1]
C0013227
UMLS CUI [6,2]
C0332256
UMLS CUI [6,3]
C0066447
exacerbation of copd, asthma (actively wheezing)
Descripción

COPD exacerbation | Asthma | Wheezing

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0740304
UMLS CUI [2]
C0004096
UMLS CUI [3]
C0043144
sinus node dysfunction in absence of pacemaker
Descripción

Sinus Node Dysfunction | Artificial cardiac pacemaker Absent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0428908
UMLS CUI [2,1]
C0030163
UMLS CUI [2,2]
C0332197
use of aggrenox (asa/dipyridamole), pentoxifylline (trental) , or oral dipyridamole (persantine)
Descripción

Aggrenox | Aspirin | Dipyridamole | Pentoxifylline | Trental | Dipyridamole Oral [Persantine]

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0732282
UMLS CUI [2]
C0004057
UMLS CUI [3]
C0012582
UMLS CUI [4]
C0030899
UMLS CUI [5]
C0699487
UMLS CUI [6]
C1242076
atrial fibrillation
Descripción

Atrial Fibrillation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004238
pregnant/breast feeding
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
non english speaking patients
Descripción

Lacking Able to speak English Language

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564215
UMLS CUI [1,3]
C0376245
subject is allergic or intolerant to aminophylline, regadenoson
Descripción

Aminophylline allergy | Intolerance to Aminophylline | Hypersensitivity Regadenoson | Intolerance to Regadenoson

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0571074
UMLS CUI [2,1]
C1744706
UMLS CUI [2,2]
C0002575
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C1698215
UMLS CUI [4,1]
C1744706
UMLS CUI [4,2]
C1698215
subject has a history of known or suspected bronchospastic lung disease [e.g., asthma, wheezing, chronic obstructive pulmonary disease (copd, etc.)]
Descripción

Lung disease Bronchial Spasm | Bronchial Spasm Suspected | Asthma | Wheezing | Chronic Obstructive Airway Disease

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0024115
UMLS CUI [1,2]
C0006266
UMLS CUI [2,1]
C0006266
UMLS CUI [2,2]
C0750491
UMLS CUI [3]
C0004096
UMLS CUI [4]
C0043144
UMLS CUI [5]
C0024117
patients with first degree or second degree av block
Descripción

First degree atrioventricular block | Second degree atrioventricular block

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085614
UMLS CUI [2]
C0264906

Similar models

Eligibility Ischemic Heart Disease NCT01137409

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
males and females age 18 through 80 years
boolean
C0001779 (UMLS CUI [1])
Gender | Female Sterilization | Hysterectomy | Bilateral tubal ligation | Postmenopausal state Duration | Pregnancy test negative
Item
female patients who are: surgically sterile (hysterectomy or bilateral tubule libation), at least one year post-menopausal, or have a negative pregnancy test on the day of treatment
boolean
C0079399 (UMLS CUI [1])
C0015787 (UMLS CUI [2])
C0020699 (UMLS CUI [3])
C0589114 (UMLS CUI [4])
C0232970 (UMLS CUI [5,1])
C0449238 (UMLS CUI [5,2])
C0427780 (UMLS CUI [6])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Food Containing Caffeine | Beverages Containing Caffeine | Pharmaceutical Preparations Containing Caffeine | Food Containing Methylxanthine | Beverages Containing Methylxanthine | Pharmaceutical Preparations Containing Methylxanthine
Item
patient consumed food/beverage/medication containing caffeine/methylxanthines up to 12 hours prior to infusion
boolean
C0016452 (UMLS CUI [1,1])
C0332256 (UMLS CUI [1,2])
C0006644 (UMLS CUI [1,3])
C0005329 (UMLS CUI [2,1])
C0332256 (UMLS CUI [2,2])
C0006644 (UMLS CUI [2,3])
C0013227 (UMLS CUI [3,1])
C0332256 (UMLS CUI [3,2])
C0006644 (UMLS CUI [3,3])
C0016452 (UMLS CUI [4,1])
C0332256 (UMLS CUI [4,2])
C0066447 (UMLS CUI [4,3])
C0005329 (UMLS CUI [5,1])
C0332256 (UMLS CUI [5,2])
C0066447 (UMLS CUI [5,3])
C0013227 (UMLS CUI [6,1])
C0332256 (UMLS CUI [6,2])
C0066447 (UMLS CUI [6,3])
COPD exacerbation | Asthma | Wheezing
Item
exacerbation of copd, asthma (actively wheezing)
boolean
C0740304 (UMLS CUI [1])
C0004096 (UMLS CUI [2])
C0043144 (UMLS CUI [3])
Sinus Node Dysfunction | Artificial cardiac pacemaker Absent
Item
sinus node dysfunction in absence of pacemaker
boolean
C0428908 (UMLS CUI [1])
C0030163 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Aggrenox | Aspirin | Dipyridamole | Pentoxifylline | Trental | Dipyridamole Oral [Persantine]
Item
use of aggrenox (asa/dipyridamole), pentoxifylline (trental) , or oral dipyridamole (persantine)
boolean
C0732282 (UMLS CUI [1])
C0004057 (UMLS CUI [2])
C0012582 (UMLS CUI [3])
C0030899 (UMLS CUI [4])
C0699487 (UMLS CUI [5])
C1242076 (UMLS CUI [6])
Atrial Fibrillation
Item
atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant/breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Lacking Able to speak English Language
Item
non english speaking patients
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Aminophylline allergy | Intolerance to Aminophylline | Hypersensitivity Regadenoson | Intolerance to Regadenoson
Item
subject is allergic or intolerant to aminophylline, regadenoson
boolean
C0571074 (UMLS CUI [1])
C1744706 (UMLS CUI [2,1])
C0002575 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1698215 (UMLS CUI [3,2])
C1744706 (UMLS CUI [4,1])
C1698215 (UMLS CUI [4,2])
Lung disease Bronchial Spasm | Bronchial Spasm Suspected | Asthma | Wheezing | Chronic Obstructive Airway Disease
Item
subject has a history of known or suspected bronchospastic lung disease [e.g., asthma, wheezing, chronic obstructive pulmonary disease (copd, etc.)]
boolean
C0024115 (UMLS CUI [1,1])
C0006266 (UMLS CUI [1,2])
C0006266 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
C0004096 (UMLS CUI [3])
C0043144 (UMLS CUI [4])
C0024117 (UMLS CUI [5])
First degree atrioventricular block | Second degree atrioventricular block
Item
patients with first degree or second degree av block
boolean
C0085614 (UMLS CUI [1])
C0264906 (UMLS CUI [2])

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