ID

33856

Description

Effects of Remote Ischemic Conditioning on Myocardial Perfusion in Humans; ODM derived from: https://clinicaltrials.gov/show/NCT02230098

Lien

https://clinicaltrials.gov/show/NCT02230098

Mots-clés

  1. 04/01/2019 04/01/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

4 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Ischemic Heart Disease NCT02230098

Eligibility Ischemic Heart Disease NCT02230098

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients referred for routine myocardial rb82-pet scanning at dept. of nuclear medicine & pet center, aarhus university hospital, skejby, denmark.
Description

RB-82 PET scan Myocardial

Type de données

boolean

Alias
UMLS CUI [1,1]
C1268555
UMLS CUI [1,2]
C0032743
UMLS CUI [1,3]
C1522564
able to understand the written patient information and to give informed consent.
Description

Comprehension Patient Information | Informed Consent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C1955348
UMLS CUI [2]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients not undergoing rb82-pet with adenosine stress test.
Description

RB-82 PET scan Absent | Stress test with adenosine Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C1268555
UMLS CUI [1,2]
C0032743
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C2036185
UMLS CUI [2,2]
C0332197
strenuous exercise (running, bicycling, fitness), intake of beta-blockers or alcohol intake on the day before and on the day of investigation.
Description

Strenuous Exercise | Running | Bicycling | Fitness | Adrenergic beta-1 Receptor Antagonists | Alcohol consumption

Type de données

boolean

Alias
UMLS CUI [1]
C1514989
UMLS CUI [2]
C0035953
UMLS CUI [3]
C0005377
UMLS CUI [4]
C1456706
UMLS CUI [5]
C0304516
UMLS CUI [6]
C0001948
pregnant/nursing women.
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
fertile women not using contraceptives.
Description

Childbearing Potential Contraceptives Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0009871
UMLS CUI [1,3]
C0332197
patients in dialysis treatment.
Description

Dialysis

Type de données

boolean

Alias
UMLS CUI [1]
C0011946
other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
Description

Comorbidity Study Subject Participation Status Inappropriate | Therapeutic procedure Study Subject Participation Status Inappropriate

Type de données

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C1548788
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C1548788
known type 2 diabetes
Description

Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011860

Similar models

Eligibility Ischemic Heart Disease NCT02230098

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
RB-82 PET scan Myocardial
Item
patients referred for routine myocardial rb82-pet scanning at dept. of nuclear medicine & pet center, aarhus university hospital, skejby, denmark.
boolean
C1268555 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C1522564 (UMLS CUI [1,3])
Comprehension Patient Information | Informed Consent
Item
able to understand the written patient information and to give informed consent.
boolean
C0162340 (UMLS CUI [1,1])
C1955348 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
RB-82 PET scan Absent | Stress test with adenosine Absent
Item
patients not undergoing rb82-pet with adenosine stress test.
boolean
C1268555 (UMLS CUI [1,1])
C0032743 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C2036185 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Strenuous Exercise | Running | Bicycling | Fitness | Adrenergic beta-1 Receptor Antagonists | Alcohol consumption
Item
strenuous exercise (running, bicycling, fitness), intake of beta-blockers or alcohol intake on the day before and on the day of investigation.
boolean
C1514989 (UMLS CUI [1])
C0035953 (UMLS CUI [2])
C0005377 (UMLS CUI [3])
C1456706 (UMLS CUI [4])
C0304516 (UMLS CUI [5])
C0001948 (UMLS CUI [6])
Pregnancy | Breast Feeding
Item
pregnant/nursing women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Childbearing Potential Contraceptives Absent
Item
fertile women not using contraceptives.
boolean
C3831118 (UMLS CUI [1,1])
C0009871 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Dialysis
Item
patients in dialysis treatment.
boolean
C0011946 (UMLS CUI [1])
Comorbidity Study Subject Participation Status Inappropriate | Therapeutic procedure Study Subject Participation Status Inappropriate
Item
other concomitant disease or treatment that according to the investigator's assessment makes the patient unsuitable for study participation.
boolean
C0009488 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
Diabetes Mellitus, Non-Insulin-Dependent
Item
known type 2 diabetes
boolean
C0011860 (UMLS CUI [1])

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