DCB-denovo: Angioplasty With Paclitaxel-coated Balloon Only Strategy for Coronary de Novo Lesions

Sponsor
Beijing Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04022200
Collaborator
(none)
300
1
48
6.3

Study Details

Study Description

Brief Summary

Drug-coating balloon (DCB) is a new interventional device for treatment of obstructive coronary artery disease (CAD). There is limited data on the long term efficacy and safety of DCB-only strategy for coronary de novo lesions in Asian patients. We therefore carry out this registry study to evaluated the clinical outcomes of paclitaxel DCB in Chinese patients in a real world medical practice.

Condition or Disease Intervention/Treatment Phase
  • Device: Paclitaxel DCB

Detailed Description

DCB has emerged as a new interventional option to treat obstructive CAD. Characterized by non-stent-based local drug delivery system, DCB has several advantages over drug-eluting stent(DES).Paclitaxel DCB inhibits excessive neointimal hyperplasia of a diseased lesions without leaving a permanent metallic frame, therefore reducing the risk of coronary thrombosis and eliminating adverse events associated with stent fracture, allergic reactions to metal struts or polymer. Since only 1 to 3 months duration of dual anti-platelet therapy(DAPT) is required after DCB intervention, the bleeding risk associated with prolonged DAPT is reduced. DCB angioplasty was proved safe in an all-comers, prospective, multicenter registry and confirmed not inferior to DES when treating small coronary lesions in a randomized clinical trial(BASKET SMALL-2). DCB has been used in"off-label"indications in the"real world" for de novo lesions, especially in vessels with diameter more than 2.75mm, and there is limited data on its long term clinical efficacy and safety in Asian patients in contemporary clinical registries. We therefore sought to evaluate the long term clinical outcome of DCB in treatment of coronary de novo lesions in Chinese patients.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Long Term Clinical Outcomes of Angioplasty With Paclitaxel-coated Balloon Only Strategy for Coronary de Novo Lesions: a Single Center Registry Study
Actual Study Start Date :
Aug 1, 2019
Anticipated Primary Completion Date :
Jan 31, 2023
Anticipated Study Completion Date :
Jul 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Paclitaxel DCB for De Novo Coronary Lesions

we define de novo coronary artery lesions as the lesions never been treated with any interventional device, such as POBA, stent, rota ablation, laser etc.

Device: Paclitaxel DCB
The length of the DCB catheter should be chosen to exceed the target lesion for at least 2mm (at both proximal and distalends). The catheter(s) will be inflated for 30 to 60s with a minimum of 7 atm. Predilation of the diseased coronary segment with a uncoated balloon/scoring balloon/cutting balloon before the use of DCB will be encouraged. DES should be implanted if the angiographic result after DCB alone therapy is not satisfactory due to significant recoil/residual stenosis or dissection (Type C-F).

Outcome Measures

Primary Outcome Measures

  1. The rate of net adverse cardiac events (NACEs) at 24 months after DCB treatment. [Clinical follow-up at 24 months after the procedure.]

    A composite endpoint of NACEs, including cardiovascular death, myocardial infarction, target lesion revascularization, target vessel revascularization, stroke, all cause bleeding.

Secondary Outcome Measures

  1. Late lumen loss(LLL) at 24 months follow-up [Coronary angiography follow-up at 24 months after the procedure.]

    LLL is defined as minimal lumen diameter(MLD) at follow-up minus MLD immediately post the procedure according to QCA.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patient-related criteria:
  • Patients with stable angina, unstable angina, myocardial infarction or evidence of asymptomatic myocardial ischemia and consent to receive coronary intervention therapy;

  • Consent to receive clinical follow up at 30 days, 3, 6, 12 and 24 months.

  • Consent to receive one angiographic follow up at 24 months after procedure.

  1. Lesion-related criteria:
  • Target coronary lesions without previous intervention therapy;

  • The lesions was intervened only with DCB;

  • The distance between other lesions requiring intervention therapy and the target lesion must >10mm.

Exclusion Criteria:
  1. Patient-related criteria:
  • Severe congestive heart failure[LVEF <30% or NYHA( New York Heart Association) III/IV)]

  • Severe valvular heart disease;

  • Pregnant or breastfeeding women;

  • Life expectancy no more than 1 year or factors causing difficulties in clinical follow up;

  • Bleeding predisposition, contraindications of anticoagulants or antiplatelet agents;

  • Intorerance to aspirin and/or clopidogrel or other anti platelet drugs;

  • Leukopenia or thrombopenia;

  • Stroke within 6 months prior to the operation;

  • A history of severe hepatic or renal failure.

  1. Lesion-related criteria :
  • Ostia lesions of left main or right coronary artery;

  • Percutaneous coronary intervention of the graft vessel;

  • Lesions that are not indications of PTCA(percutaneous transluminal coronary angiography) or other intervention therapy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Beijing Hospital Beijing Beijing China 100730

Sponsors and Collaborators

  • Beijing Hospital

Investigators

  • Study Chair: Xue Yu, MD, Beijing Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Xue Yu, Vice Director of Cardiology Department, Beijing Hospital
ClinicalTrials.gov Identifier:
NCT04022200
Other Study ID Numbers:
  • BJH DCB for de novo
First Posted:
Jul 17, 2019
Last Update Posted:
Mar 22, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xue Yu, Vice Director of Cardiology Department, Beijing Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2022