ID

20524

Description

The Efficacy of CILostazol ON Ischemic Complications After DES Implantation; ODM derived from: https://clinicaltrials.gov/show/NCT00776828

Lien

https://clinicaltrials.gov/show/NCT00776828

Mots-clés

Versions (1)
  1. 01/03/2017 01/03/2017 -
Téléchargé le

1 mars 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

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Eligibility Coronary Artery Disease NCT00776828

Anglais

Eligibility Coronary Artery Disease NCT00776828

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
subject must be at leat 18 years of age
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of cilostazol and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
subject must have significant coronary artery stenosis (>50% by visual estimate)
Description

Coronary Stenosis Percentage Visual estimation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C0439165
UMLS CUI [1,3]
C0444684
subject must have evidence of myocardial ischemia (e.g., stable, unstable angina, recent infarction, silent ischemia, positive functional study or reversible changes in the electrocardiogram (ecg) consistent with ischemia. in subjects with coronary artery stenosis>75%, evidence of myocardial ischemia does not have to be documented.
Description

Myocardial Ischemia; Stable angina; Angina, Unstable; History of myocardial infarction; Silent myocardial ischemia; ECG signs of myocardial ischaemia; Coronary Stenosis

Type de données

boolean

Alias
UMLS CUI [1,1]
C0151744
UMLS CUI [1,2]
C0340288
UMLS CUI [1,3]
C0002965
UMLS CUI [1,4]
C1275835
UMLS CUI [1,5]
C0340291
UMLS CUI [1,6]
C1141959
UMLS CUI [1,7]
C0242231
coronary lesions must be amenable for percutaneous coronary revascularization with drug eluting stents.
Description

coronary stenosis amenable for percutaneous coronary revascularization with drug eluting stents

Type de données

boolean

Alias
UMLS CUI [1,1]
C0242231
UMLS CUI [1,2]
C3526701
UMLS CUI [1,3]
C1262327
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject who undergoes primary percutaneous coronary intervention due to acute st elevation myocardial infarction
Description

Emergency percutaneous coronary intervention; Acute ST segment elevation myocardial infarction

Type de données

boolean

Alias
UMLS CUI [1,1]
C1532297
UMLS CUI [1,2]
C1303258
subject who has contraindication or allergy to anti-platelet agents (aspirin, clopidogrel or cilostazol)
Description

hypersensitivity or contraindication to anti-platelet agents (aspirin, clopidogrel or cilostazol)

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C2963157
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0004057
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0070166
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0055729
subject who has thrombocytopenia (<120,000/ul)
Description

platelet count measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0032181
subject who has liver cirrhosis (child class b or c)
Description

liver cirrhosis

Type de données

boolean

Alias
UMLS CUI [1]
C0023890
subject who is on the anticoagulation therapy
Description

anticoagulation

Type de données

boolean

Alias
UMLS CUI [1]
C0449867
subject who has severe congestive heart failure (left ventricular ejection fraction <30%)
Description

congestive heart failure, left ventricular ejection fraction

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0428772
Retour au début de la page

Similar models

Eligibility Coronary Artery Disease NCT00776828

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
subject must be at leat 18 years of age
boolean
C0001779 (UMLS CUI [1])
informed consent
Item
subject is able to verbally confirm understandings of risks, benefits and treatment alternatives of cilostazol and he/she or his/her legally authorized representative provides written informed consent prior to any study related procedure.
boolean
C0021430 (UMLS CUI [1])
Coronary Stenosis Percentage Visual estimation
Item
subject must have significant coronary artery stenosis (>50% by visual estimate)
boolean
C0242231 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C0444684 (UMLS CUI [1,3])
Myocardial Ischemia; Stable angina; Angina, Unstable; History of myocardial infarction; Silent myocardial ischemia; ECG signs of myocardial ischaemia; Coronary Stenosis
Item
subject must have evidence of myocardial ischemia (e.g., stable, unstable angina, recent infarction, silent ischemia, positive functional study or reversible changes in the electrocardiogram (ecg) consistent with ischemia. in subjects with coronary artery stenosis>75%, evidence of myocardial ischemia does not have to be documented.
boolean
C0151744 (UMLS CUI [1,1])
C0340288 (UMLS CUI [1,2])
C0002965 (UMLS CUI [1,3])
C1275835 (UMLS CUI [1,4])
C0340291 (UMLS CUI [1,5])
C1141959 (UMLS CUI [1,6])
C0242231 (UMLS CUI [1,7])
coronary stenosis amenable for percutaneous coronary revascularization with drug eluting stents
Item
coronary lesions must be amenable for percutaneous coronary revascularization with drug eluting stents.
boolean
C0242231 (UMLS CUI [1,1])
C3526701 (UMLS CUI [1,2])
C1262327 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Emergency percutaneous coronary intervention; Acute ST segment elevation myocardial infarction
Item
subject who undergoes primary percutaneous coronary intervention due to acute st elevation myocardial infarction
boolean
C1532297 (UMLS CUI [1,1])
C1303258 (UMLS CUI [1,2])
hypersensitivity or contraindication to anti-platelet agents (aspirin, clopidogrel or cilostazol)
Item
subject who has contraindication or allergy to anti-platelet agents (aspirin, clopidogrel or cilostazol)
boolean
C0020517 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C2963157 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C0004057 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0070166 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0055729 (UMLS CUI [4,2])
platelet count measurement
Item
subject who has thrombocytopenia (<120,000/ul)
boolean
C0032181 (UMLS CUI [1])
liver cirrhosis
Item
subject who has liver cirrhosis (child class b or c)
boolean
C0023890 (UMLS CUI [1])
anticoagulation
Item
subject who is on the anticoagulation therapy
boolean
C0449867 (UMLS CUI [1])
congestive heart failure, left ventricular ejection fraction
Item
subject who has severe congestive heart failure (left ventricular ejection fraction <30%)
boolean
C0018802 (UMLS CUI [1,1])
C0428772 (UMLS CUI [1,2])
Retour au début de la page 

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