Age
Item
1. 18yrs≤age≤75yrs .
boolean
C0001779 (UMLS CUI [1])
Lesion de novo | Coronary artery Native
Item
2. de novo lesion at native coronary artery.
boolean
C0221198 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C0205042 (UMLS CUI [2,1])
C0302891 (UMLS CUI [2,2])
Target vessel Single | Target Lesion Single
Item
3. single target vessel and single target lesion.
boolean
C0449618 (UMLS CUI [1,1])
C0205171 (UMLS CUI [1,2])
C2986546 (UMLS CUI [2,1])
C0205171 (UMLS CUI [2,2])
Lesion Length
Item
4. lesion length ≤32mm.
boolean
C0221198 (UMLS CUI [1,1])
C1444754 (UMLS CUI [1,2])
Reference Vessel Diameter
Item
5. rvd 2.5mm~4.0mm.
boolean
C1706462 (UMLS CUI [1,1])
C0005847 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,3])
Percent Diameter Stenosis Measurement Visual estimation
Item
6. ds%≥70% by visual estimation.
boolean
C3897965 (UMLS CUI [1,1])
C0444684 (UMLS CUI [1,2])
Target Lesion Covered | Stent Quantity
Item
7. target lesion could be covered by only one stent.
boolean
C2986546 (UMLS CUI [1,1])
C1999244 (UMLS CUI [1,2])
C0038257 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
Compliance behavior Follow-up
Item
8. subjects are willing to follow the specified requirements follow-up.
boolean
C1321605 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
Informed Consent
Item
9. a process by which a subject voluntarily confirms his or her willingness to participate in a particular trial, after having been informed of all aspects of the trial that are relevant to the subject's decision to participate. informed consent is documented by means of a written, signed and dated informed consent form.
boolean
C0021430 (UMLS CUI [1])
Recent myocardial infarction
Item
1. ami within one week.
boolean
C1998297 (UMLS CUI [1])
Chronic Total Occlusion Vessel TIMI grade | Left main coronary artery Lesion | Ostium Lesion | Graft Vessel Lesion | Bifurcation Lesion | In Stent restenosis | Multiple Vessel Disease
Item
2. cto(timi0),lm lesion,ostial lesion,graft vessel lesion,bifurcation (side branch rvd≥2.5mm),isr,mutivessel disease need to be treated.
boolean
C3275069 (UMLS CUI [1,1])
C4263591 (UMLS CUI [1,2])
C1261082 (UMLS CUI [2,1])
C0221198 (UMLS CUI [2,2])
C0444567 (UMLS CUI [3,1])
C0221198 (UMLS CUI [3,2])
C0332835 (UMLS CUI [4,1])
C0005847 (UMLS CUI [4,2])
C0221198 (UMLS CUI [4,3])
C3146289 (UMLS CUI [5,1])
C0221198 (UMLS CUI [5,2])
C3272317 (UMLS CUI [6])
C0005847 (UMLS CUI [7,1])
C0439064 (UMLS CUI [7,2])
C0012634 (UMLS CUI [7,3])
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])
Lesion Inadequate Placement of stent
Item
4. extremely tortuous proximal to the lesion that is inadequate to stent delivery.
boolean
C0221198 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
C0522776 (UMLS CUI [1,3])
New York Heart Association Classification | Left ventricular ejection fraction
Item
5. nyha≥ⅲ or lvef≤40%.
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 Planned Postoperative
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])
C1301732 (UMLS CUI [4,2])
C0032790 (UMLS CUI [4,3])
Bleeding tendency | Blood Coagulation Disorders | Medical contraindication Percutaneous Coronary Intervention | Taboo Anticoagulant therapy | Dual Antiplatelet therapy Discontinue Unable
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])
C0039227 (UMLS CUI [4,1])
C0150457 (UMLS CUI [4,2])
C1096021 (UMLS CUI [5,1])
C0205173 (UMLS CUI [5,2])
C1444662 (UMLS CUI [5,3])
C1299582 (UMLS CUI [5,4])
Malignant Neoplasms | Congestive heart failure | Organ Transplantation | Organ Transplantation Scheduled | Substance Use Disorders | Poor compliance | Life Expectancy Limited
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])
C0205539 (UMLS CUI [4,2])
C0038586 (UMLS CUI [5])
C0032646 (UMLS CUI [6])
C0023671 (UMLS CUI [7,1])
C0439801 (UMLS CUI [7,2])
Aspirin allergy | Heparin allergy | Hypersensitivity Clopidogrel | Hypersensitivity Cobalt | Hypersensitivity Chromium Alloys | Hypersensitivity Sirolimus | Hypersensitivity Polylactic acid | Contrast media allergy
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])
C0009148 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0008575 (UMLS CUI [5,2])
C0020517 (UMLS CUI [6,1])
C0072980 (UMLS CUI [6,2])
C0020517 (UMLS CUI [7,1])
C0071443 (UMLS CUI [7,2])
C0570562 (UMLS CUI [8])
Liver Dysfunction Serious | Renal Insufficiency Serious
Item
11. serious liver and kidney function is not complete person.
boolean
C0086565 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C1565489 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
Study Subject Participation Status Inappropriate
Item
12. the investigators think that do not fit to enroll the study.
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])