Status:
UNKNOWN
Paclitaxel Eluting Balloon Catheter in Coronary De-novo Lesions Treatment in China
Lead Sponsor:
Xijing Hospital
Collaborating Sponsors:
The First Affiliated Hospital of Zhengzhou University
First Affiliated Hospital of Zhejiang University
Conditions:
Coronary Disease
Eligibility:
All Genders
18-78 years
Phase:
NA
Brief Summary
The aim of this Real-world study in China is evaluating the Safety and Efficacy of Paclitaxel Eluting Balloon Catheter in Coronary de-novo lesions(target vessel diameter:2.5mm-4.0mm)Treatment. And the...
Eligibility Criteria
Inclusion
- 18-78 years of age, male or non-pregnant female;
- patients with asymptomatic or symptomatic myocardial ischemia, stable or unstable angina pectoris, myocardial infarction with a course of more than two weeks, and patients with indications for percutaneous coronary intervention;
- the target lesions were primary, in situ coronary artery stenosis, located on one or two different coronary artery vessels, the number of target lesions on each coronary artery was not more than one;
- the length of the target lesion ≤ 26mm (visual), which can be covered by a single drug balloon (it is suggested that the balloon should cover at least 4mm healthy partition, 2 mm at each end; The reference diameter of target vessel was 2.5mm-4.0mm (visual);
- the stenosis degree of the target lesion was ≥ 70%;
- left ventricular ejection fraction ≥ 45%.
- patients who can understand the purpose of the trial, voluntarily participate and sign informed consent, and are willing to follow up the study.
Exclusion
- Related to patients:
- patients with myocardial infarction within two weeks;
- pregnant or lactating women;
- cardiogenic shock, acute infection, known bleeding or coagulation disorder, or active digestive tract; Patients with history of hemorrhage or ulcer, cerebral hemorrhage or subarachnoid hemorrhage, stroke within half a year;
- patients with a life expectancy less than one year or with difficulties in clinical follow-up;
- patients who had a history of PTCA or had other operations scheduled during the follow-up period of one year;
- patients who are participating in any other clinical study and who have not reached the main end point of the study;
- present or previous history of severe liver disease, and / or renal impairment: serum creatinine \> 2.0 mg / dl( 176.8 umol / L) or undergoing hemodialysis therapy. Therefore, it does not meet the requirements of angiography;
- patients with left ventricular ejection fraction below 45%;
- for other reasons, the researchers did not think it was appropriate for a patient to be selected.
- Related to lesions:
- left main lesion and the bifurcation with side branch \>2.5 mm;
- the location of the lesion was less than 10 mm at the proximal end of the anterior descending branch, 5 mm in the circumflex branch and 5 mm in the proximal end of the right coronary artery.
- severe calcification and twisted lesions which can not be successfully predilated, are not suitable for drug balloon delivery and expansion.
- lesion length ≥ 26 mm;
- evidence of severe thrombosis in target vessels before intervention;
- lesions that cannot be treated with PTCA or other interventional techniques;
- after predilation of the target lesion, residual stenosis ≥ 30% or TIMI blood flow \< 3, and / or obvious flow limiting dissection.
- Exclusion criteria related to drugs:
- patients with bleeding constitution, anticoagulant or antiplatelet drugs;
- patients who cannot tolerate aspirin and / or clopidogrel or who have a history of neutropenia or thrombocytopenia or who have too severe liver failure to receive clopidogrel;
- patients known to be intolerant or allergic to heparin, contrast agents, paclitaxel, iopramide, rapamycin, polylactic acid-glycolic acid polymer, stainless steel, etc.
- leukopenia (leukocyte count \< 3 × 109 / L and the course \> 3 days) or neutropenia ANC \< 1000 neutrophil / mm3 and the course\> 3 days). Or patients had a history of thrombocytopenia (\< 100,000 platelets / mm3;
- patients with a history of peptic ulcer or gastrointestinal bleeding in the past 6 months.
Key Trial Info
Start Date :
February 22 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2020
Estimated Enrollment :
600 Patients enrolled
Trial Details
Trial ID
NCT03466749
Start Date
February 22 2018
End Date
December 31 2020
Last Update
April 12 2019
Active Locations (1)
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1
Ling Tao
Xi'an, Shannxi, China, 710032