Informationen:
Fehler:
ID
33856
Beschreibung
Effects of Remote Ischemic Conditioning on Myocardial Perfusion in Humans; ODM derived from: https://clinicaltrials.gov/show/NCT02230098
Link
https://clinicaltrials.gov/show/NCT02230098
Stichworte
Versionen (1)
- 04.01.19 04.01.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
4. Januar 2019
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Ischemic Heart Disease NCT02230098
Eligibility Ischemic Heart Disease NCT02230098
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Ischemic Heart Disease NCT02230098
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
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])
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])
C1955348 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
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])
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])
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])
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])
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])
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])
Keine Kommentare