ID

40480

Beschreibung

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

Stichworte

Versionen (1)
  1. 25.04.20 25.04.20 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

25. April 2020

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Ischemic Heart Disease NCT01137409

Englisch

Eligibility Ischemic Heart Disease NCT01137409

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

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

Age

Datentyp

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
Beschreibung

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

Datentyp

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
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

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

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

Datentyp

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)
Beschreibung

COPD exacerbation | Asthma | Wheezing

Datentyp

boolean

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

Sinus Node Dysfunction | Artificial cardiac pacemaker Absent

Datentyp

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)
Beschreibung

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

Datentyp

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
Beschreibung

Atrial Fibrillation

Datentyp

boolean

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

Pregnancy | Breast Feeding

Datentyp

boolean

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

Lacking Able to speak English Language

Datentyp

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
Beschreibung

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

Datentyp

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.)]
Beschreibung

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

Datentyp

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
Beschreibung

First degree atrioventricular block | Second degree atrioventricular block

Datentyp

boolean

Alias
UMLS CUI [1]
C0085614
UMLS CUI [2]
C0264906
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Ischemic Heart Disease NCT01137409

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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