Eligibility Coronary Artery Disease NCT02027870

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StudyEvent: Eligibility
1. Eligibility Coronary Artery Disease NCT02027870

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de dados

Alias

Inclusion Criteria

Item Group

C1512693 (UMLS CUI)

Item

1.18yrs≤age≤75yrs . 2..stability and unstable angina pectoris (ap), chronic myocardial infarction (omi) or confirmed (myocardial ischemia; 3.de novo lesion at native coronary artery(up to four target lesions). 4.lesion length ≤60mm. 5.rvd 2.25mm～4.0mm. 6.ds%≥70% by visual estimation. 7.coronary artery bypass surgery (coronary artery bypass grafting) patients. 8.subjects are willing to follow the specified requirements follow-up.

boolean

C0001779 (UMLS CUI [1])
C0340288 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C1392608 (UMLS CUI [4])
C0151744 (UMLS CUI [5])
C0221198 (UMLS CUI [6,1])
C1515568 (UMLS CUI [6,2])
C0205042 (UMLS CUI [6,3])
C0302891 (UMLS CUI [6,4])
C2986546 (UMLS CUI [7,1])
C1265611 (UMLS CUI [7,2])
C0221198 (UMLS CUI [8,1])
C1444754 (UMLS CUI [8,2])
C1706462 (UMLS CUI [9,1])
C0005847 (UMLS CUI [9,2])
C1301886 (UMLS CUI [9,3])
C3897965 (UMLS CUI [10])
C0010055 (UMLS CUI [11])
C1510802 (UMLS CUI [12,1])
C3274571 (UMLS CUI [12,2])

Comprehension Testing | Informed Consent | Protocol Compliance

Item

9.to understand the purpose of testing, voluntary and signed informed consent, willing to accept the imaging and clinical follow-up of subjects.

boolean

C0162340 (UMLS CUI [1,1])
C0039593 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
C0525058 (UMLS CUI [3])

Exclusion Criteria

Item Group

C0680251 (UMLS CUI)

Acute myocardial infarction

Item

1. ami within 7 days.

boolean

C0155626 (UMLS CUI [1])

Left coronary artery main stem Lesion | Transplant Vasculopathy | Stent restenosis Lesion

Item

2. left main lesion, transplant vasculopathy and stent restenosis lesion;

boolean

C0226031 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C0040732 (UMLS CUI [2,1])
C0042373 (UMLS CUI [2,2])
C3272317 (UMLS CUI [3,1])
C0221198 (UMLS CUI [3,2])

Lesion Calcified Severe

Item

3. severe calcified lesion unable to predilate.

boolean

C0221198 (UMLS CUI [1,1])
C0175895 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])

Stent Distortion Interfered by Lesion

Item

4. the distortion of the stent was hampered by lesions.

boolean

C1710193 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0221198 (UMLS CUI [1,3])

New York Heart Association Classification | Left ventricular ejection fraction

Item

5. nyha≥ⅲ or lvef＜35%.

boolean

C1275491 (UMLS CUI [1])
C0428772 (UMLS CUI [2])

Stenting Previous

Item

6. prior stenting within 1 year.

boolean

C2348535 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])

Pregnancy | Breast Feeding | Planned Pregnancy Postoperative | Breast Feeding Postoperative Planned

Item

7. pregnancy or lactation, and plan in postoperative pregnancy or lactation.

boolean

C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3,1])
C0032790 (UMLS CUI [3,2])
C0006147 (UMLS CUI [4,1])
C0032790 (UMLS CUI [4,2])
C1301732 (UMLS CUI [4,3])

Bleeding tendency | Blood Coagulation Disorders | Medical contraindication PCI | Anticoagulant therapy Taboo | Dual Antiplatelet therapy Continue Unsuccessful

Item

8. subjects had bleeding tendency or blood coagulation dysfunction or pci contraindications, or anticoagulant therapy taboo or can't continue dapt healers at least 1 year.

boolean

C1458140 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
C1301624 (UMLS CUI [3,1])
C1532338 (UMLS CUI [3,2])
C0150457 (UMLS CUI [4,1])
C0039227 (UMLS CUI [4,2])
C1096021 (UMLS CUI [5,1])
C0205173 (UMLS CUI [5,2])
C0549178 (UMLS CUI [5,3])
C1272705 (UMLS CUI [5,4])

Item

9. there are other diseases (such as cancer,malignant tumor ,congestive heart failure,organ transplantation or candidate) or abuse history (alcohol cocaine heroin, etc.), scheme compliance is poor, interference related data explanation or the limited life (< 1 year).

boolean

C0006826 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
C0029216 (UMLS CUI [3])
C0029216 (UMLS CUI [4,1])
C3840775 (UMLS CUI [4,2])
C0038586 (UMLS CUI [5])
C0032646 (UMLS CUI [6])
C0521102 (UMLS CUI [7,1])
C0681841 (UMLS CUI [7,2])
C0681873 (UMLS CUI [7,3])
C0023671 (UMLS CUI [8,1])
C0439801 (UMLS CUI [8,2])

Item

10. to aspirin heparin clopidogrel cobalt chromium alloy rapamycin pla polymer contrast agent of one of allergy.

boolean

C0004058 (UMLS CUI [1])
C0571776 (UMLS CUI [2])
C0020517 (UMLS CUI [3,1])
C0070166 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0008576 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0072980 (UMLS CUI [5,2])
C0020517 (UMLS CUI [6,1])
C0071443 (UMLS CUI [6,2])
C0032521 (UMLS CUI [6,3])
C0570562 (UMLS CUI [7])

Liver function Serious | Renal function Serious | Alanine aminotransferase increased | Aspartate aminotransferase increased

Item

11. serious liver and kidney function is not complete person(alt and ast were three times greater than the upper limit of normal).

boolean

C0232741 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0232804 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0151905 (UMLS CUI [3])
C0151904 (UMLS CUI [4])

Study Subject Participation Status

Item

12. rounding out the top participated in other clinical trials have not reached the main research the finish time limit.

boolean

C2348568 (UMLS CUI [1])

Poor compliance | Completion of clinical trial failed

Item

13. the researchers determine adherence is poor, could not finish my study in accordance with the requirements of the subjects.

boolean

C0032646 (UMLS CUI [1])
C2732579 (UMLS CUI [2,1])
C0231175 (UMLS CUI [2,2])

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Eligibility Coronary Artery Disease NCT02027870