ID

28715

Description

The EFFect of hIgh Dose ClopIdogrel treatmENT in Patients With Clopidogrel Resistance; ODM derived from: https://clinicaltrials.gov/show/NCT01032668

Link

https://clinicaltrials.gov/show/NCT01032668

Keywords

  1. 1/26/18 1/26/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 26, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Coronary Artery Disease NCT01032668

Eligibility Coronary Artery Disease NCT01032668

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patients; who have planned elective pci and have had written informed consent for participation to study.
Description

Percutaneous Coronary Intervention elective Planned | Informed Consent

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0439608
UMLS CUI [1,3]
C1301732
UMLS CUI [2]
C0021430
age>18 year-old,
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
the native coronary artery;lesion with narrowing >=70%
Description

Coronary artery Native | Lesion Stenosis Percentage

Data type

boolean

Alias
UMLS CUI [1,1]
C0205042
UMLS CUI [1,2]
C0302891
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C1261287
UMLS CUI [2,3]
C0439165
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients have allergy for asa, clopidogrel and heparin
Description

Aspirin allergy | Hypersensitivity clopidogrel | Heparin allergy

Data type

boolean

Alias
UMLS CUI [1]
C0004058
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0070166
UMLS CUI [3]
C0571776
patients who performed primary pci
Description

Percutaneous Coronary Intervention Primary

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0205225
patients with acute coronary syndrome
Description

Acute Coronary Syndrome

Data type

boolean

Alias
UMLS CUI [1]
C0948089
patients with have a history of pci and use clopidogrel
Description

History Percutaneous Coronary Intervention | Clopidogrel Use of

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C1532338
UMLS CUI [2,1]
C0070166
UMLS CUI [2,2]
C1524063
patients on warfarin therapy
Description

Warfarin

Data type

boolean

Alias
UMLS CUI [1]
C0043031
patients who have bleeding diathesis, or have high risk for bleeding.
Description

Bleeding tendency | High risk of bleeding

Data type

boolean

Alias
UMLS CUI [1]
C1458140
UMLS CUI [2]
C4039184

Similar models

Eligibility Coronary Artery Disease NCT01032668

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Percutaneous Coronary Intervention elective Planned | Informed Consent
Item
the patients; who have planned elective pci and have had written informed consent for participation to study.
boolean
C1532338 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2])
Age
Item
age>18 year-old,
boolean
C0001779 (UMLS CUI [1])
Coronary artery Native | Lesion Stenosis Percentage
Item
the native coronary artery;lesion with narrowing >=70%
boolean
C0205042 (UMLS CUI [1,1])
C0302891 (UMLS CUI [1,2])
C0221198 (UMLS CUI [2,1])
C1261287 (UMLS CUI [2,2])
C0439165 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Aspirin allergy | Hypersensitivity clopidogrel | Heparin allergy
Item
patients have allergy for asa, clopidogrel and heparin
boolean
C0004058 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0070166 (UMLS CUI [2,2])
C0571776 (UMLS CUI [3])
Percutaneous Coronary Intervention Primary
Item
patients who performed primary pci
boolean
C1532338 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Acute Coronary Syndrome
Item
patients with acute coronary syndrome
boolean
C0948089 (UMLS CUI [1])
History Percutaneous Coronary Intervention | Clopidogrel Use of
Item
patients with have a history of pci and use clopidogrel
boolean
C0262926 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C0070166 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
Warfarin
Item
patients on warfarin therapy
boolean
C0043031 (UMLS CUI [1])
Bleeding tendency | High risk of bleeding
Item
patients who have bleeding diathesis, or have high risk for bleeding.
boolean
C1458140 (UMLS CUI [1])
C4039184 (UMLS CUI [2])

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