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ID
16471
Beschreibung
Rapamycin+Estradiol- vs. Rapamycin-Eluting Stents to Reduce Restenosis (ISAR-PEACE); ODM derived from: https://clinicaltrials.gov/show/NCT00402636
Link
https://clinicaltrials.gov/show/NCT00402636
Stichworte
Versionen (2)
- 17.07.16 17.07.16 -
- 21.07.16 21.07.16 - Julian Varghese
Hochgeladen am
17. Juli 2016
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Eligibility Coronary Heart Disease NCT00402636
Eligibility Coronary Heart Disease NCT00402636
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Coronary Heart Disease NCT00402636
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age, ischemic symptoms or evidence of myocardial ischemia, coronary vessel stenosis
Item
patients older than age 18 with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥50% de novo stenosis located in native coronary vessels.
boolean
C0001779 (UMLS CUI [1])
C0151744 (UMLS CUI [2])
C0242231 (UMLS CUI [3])
C0151744 (UMLS CUI [2])
C0242231 (UMLS CUI [3])
informed consent
Item
written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
boolean
C0021430 (UMLS CUI [1])
target lesion located in the left main trunk or bypass graft
Item
target lesion located in the left main trunk or bypass graft.
boolean
C2184261 (UMLS CUI [1,1])
C0226069 (UMLS CUI [1,2])
C2184261 (UMLS CUI [2,1])
C0185098 (UMLS CUI [2,2])
C0226069 (UMLS CUI [1,2])
C2184261 (UMLS CUI [2,1])
C0185098 (UMLS CUI [2,2])
In-stent restenosis
Item
in-stent restenosis.
boolean
C3272317 (UMLS CUI [1])
acute st-elevation myocardial infarction
Item
acute st-elevation myocardial infarction.
boolean
C1303258 (UMLS CUI [1])
Cardiogenic shock
Item
cardiogenic shock.
boolean
C0036980 (UMLS CUI [1])
Comorbidity
Item
malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Allergy to the study medications
Item
known allergy to the study medications: aspirin, clopidogrel, rapamycin, estradiol, stainless steel.
boolean
C0020517 (UMLS CUI [1,1])
C3854006 (UMLS CUI [1,2])
C3854006 (UMLS CUI [1,2])
Pregnancy
Item
pregnancy (present, suspected or planned) or positive pregnancy test.
boolean
C0032961 (UMLS CUI [1])
Previous enrollment in this trial
Item
previous enrollment in this trial.
boolean
C2348568 (UMLS CUI [1])
inability to cooperate with the study protocol
Item
patient's inability to fully cooperate with the study protocol.
boolean
C2348563 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])