ID

16471

Beschrijving

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

Trefwoorden

Versies (2)
  1. 17-07-16 17-07-16 -
  2. 21-07-16 21-07-16 - Julian Varghese
Geüploaded op

17 juli 2016

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Coronary Heart Disease NCT00402636

Engels

Eligibility Coronary Heart Disease NCT00402636

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
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.
Beschrijving

Age, ischemic symptoms or evidence of myocardial ischemia, coronary vessel stenosis

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0151744
UMLS CUI [3]
C0242231
written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
target lesion located in the left main trunk or bypass graft.
Beschrijving

target lesion located in the left main trunk or bypass graft

Datatype

boolean

Alias
UMLS CUI [1,1]
C2184261
UMLS CUI [1,2]
C0226069
UMLS CUI [2,1]
C2184261
UMLS CUI [2,2]
C0185098
in-stent restenosis.
Beschrijving

In-stent restenosis

Datatype

boolean

Alias
UMLS CUI [1]
C3272317
acute st-elevation myocardial infarction.
Beschrijving

acute st-elevation myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1]
C1303258
cardiogenic shock.
Beschrijving

Cardiogenic shock

Datatype

boolean

Alias
UMLS CUI [1]
C0036980
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.
Beschrijving

Comorbidity

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
known allergy to the study medications: aspirin, clopidogrel, rapamycin, estradiol, stainless steel.
Beschrijving

Allergy to the study medications

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C3854006
pregnancy (present, suspected or planned) or positive pregnancy test.
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
previous enrollment in this trial.
Beschrijving

Previous enrollment in this trial

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
patient's inability to fully cooperate with the study protocol.
Beschrijving

inability to cooperate with the study protocol

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C0439801
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Similar models

Eligibility Coronary Heart Disease NCT00402636

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
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])
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