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Rivaroxaban Combined With DAPT Versus DAPT Alone After Drug-coated Balloon Angioplasty

Primary Purpose

Acute Coronary Syndrome

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
rivaroxaban
Sponsored by
Henan Institute of Cardiovascular Epidemiology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Coronary Syndrome

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: ACS patients who meet the indications of percutaneous coronary intervention The reference diameter of the target vessel was ≥2.75mm Target lesions were treated with a drug-coated balloon catheter (DCB) for PCI According to IVUS assessment, the target lesions were dissected and accumulated medium without affecting distal blood flow Exclusion Criteria: <18 or >60 years old Bridging vessels or stent restenosis Unable to sign written informed consent Female patients during pregnancy or lactation (for women who have not stopped menstruation, pregnancy test should be performed within 7 days prior to enrollment in this study) Antiplatelet agents and anticoagulants are not available; Have heparin, contrast agent and other allergies The subjects were participating in other uncompleted clinical trials Scheduled elective surgery Life expectancy is less than 1 year Patients with high blood risk Has long-term oral anticoagulant therapy adaptation Cardiogenic shock Patients with severe intraoperative dissection or hematoma requiring stent rescue

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    DAPT+rivaroxaban

    DAPT

    Arm Description

    Rivaroxaban 2.5 mg bid + aspirin 100 mg qd + ticagrelor 90 mg bid was used for 1 month after operation, and then aspirin 100 mg + ticagrelor 90 mg bid was used for 5 months.

    aspirin 100 mg qd + ticagrelor 90 mg bid for 6 months.

    Outcomes

    Primary Outcome Measures

    Loss of lumen area of target vessel
    Evaluation of postoperative target vessel MLA minus MLA at follow-up using IVUS

    Secondary Outcome Measures

    Vascular dissection healing
    Re-use IVUS to evaluate the vascular reexamination of the original dissection
    Minimum lumen area
    using IVUS
    Cardiovascular death
    All deaths are counted as cardiovascular deaths unless there is a clear determination of other causes
    Target vessel myocardial infarction
    CAG confirms
    Clinical-driven revascularization of target lesions
    Type 3 or 5 bleeding events defined by BARC

    Full Information

    First Posted
    February 20, 2023
    Last Updated
    February 20, 2023
    Sponsor
    Henan Institute of Cardiovascular Epidemiology
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05750758
    Brief Title
    Rivaroxaban Combined With DAPT Versus DAPT Alone After Drug-coated Balloon Angioplasty
    Official Title
    A Randomized Controlled Trial of Rivaroxaban Combined With Dual Antiplatelet Therapy Versus Dual Antiplatelet Therapy Alone 1 Month After Drug-coated Balloon Angioplasty in Patients With Acute Coronary Syndrome Without High Bleeding Risk
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    February 20, 2023 (Anticipated)
    Primary Completion Date
    December 1, 2023 (Anticipated)
    Study Completion Date
    April 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Henan Institute of Cardiovascular Epidemiology

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The target population of this interventional study was ACS patients with drug-coated balloons. The main discussion : 1.1 months of rivaroxaban combined with dual antiplatelet therapy compared with dual antiplatelet therapy alone, late lumen loss at 6 months. 2. To determine the safety of the regimen with bleeding events as the end point. Subjects were randomly assigned to two groups, one receiving routine DAPT for six months and one receiving DAPT plus one month of rivaroxaban 2.5 mg bid
    Detailed Description
    Drug-coated balloon ( DCB ) is to apply anti-intimal hyperplasia drugs to the surface of the balloon. When the balloon reaches the diseased blood vessel and is stretched and expanded, it contacts the intima of the blood vessel wall. By tearing the intima of the blood vessel and pressing, the transfer drug is quickly released to the intima of the blood vessel, thereby preventing restenosis after vascular intervention. Pretreatment is a key step in the use of drug balloons in situ macroangiopathy. At present, it is required that the residual stenosis of the lesion during pretreatment is ≤ 30 %, and there is no distal blood flow restrictive dissection and hematoma. The relationship between dissection hematoma and residual stenosis is difficult to deal with. Some small dissections are beneficial to the absorption of DCB anti-proliferative drugs by the vascular wall. The larger dissection may cause the thrombus to persist in the vascular wall, resulting in late lumen loss after organization. Rivaroxaban is a new oral anticoagulant, which is gradually used in the treatment of coronary heart disease. At present, there is no clinical study on the prognosis of vascular dissection in DCB. Based on the above research background, we designed the following trial, aimed to study in ACS population, vascular lumen access + hemorrhagic events as the end point, try to clear 1 month rivaroxaban combined with dual antiplatelet therapy compared with single dual antiplatelet therapy effect.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Coronary Syndrome

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    DAPT+rivaroxaban
    Arm Type
    Experimental
    Arm Description
    Rivaroxaban 2.5 mg bid + aspirin 100 mg qd + ticagrelor 90 mg bid was used for 1 month after operation, and then aspirin 100 mg + ticagrelor 90 mg bid was used for 5 months.
    Arm Title
    DAPT
    Arm Type
    No Intervention
    Arm Description
    aspirin 100 mg qd + ticagrelor 90 mg bid for 6 months.
    Intervention Type
    Drug
    Intervention Name(s)
    rivaroxaban
    Intervention Description
    rivaroxaban 2.5mg bid for 1m
    Primary Outcome Measure Information:
    Title
    Loss of lumen area of target vessel
    Description
    Evaluation of postoperative target vessel MLA minus MLA at follow-up using IVUS
    Time Frame
    6 months
    Secondary Outcome Measure Information:
    Title
    Vascular dissection healing
    Description
    Re-use IVUS to evaluate the vascular reexamination of the original dissection
    Time Frame
    6 months
    Title
    Minimum lumen area
    Description
    using IVUS
    Time Frame
    6 months
    Title
    Cardiovascular death
    Description
    All deaths are counted as cardiovascular deaths unless there is a clear determination of other causes
    Time Frame
    6 months
    Title
    Target vessel myocardial infarction
    Description
    CAG confirms
    Time Frame
    6 months
    Title
    Clinical-driven revascularization of target lesions
    Time Frame
    6 months
    Title
    Type 3 or 5 bleeding events defined by BARC
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: ACS patients who meet the indications of percutaneous coronary intervention The reference diameter of the target vessel was ≥2.75mm Target lesions were treated with a drug-coated balloon catheter (DCB) for PCI According to IVUS assessment, the target lesions were dissected and accumulated medium without affecting distal blood flow Exclusion Criteria: <18 or >60 years old Bridging vessels or stent restenosis Unable to sign written informed consent Female patients during pregnancy or lactation (for women who have not stopped menstruation, pregnancy test should be performed within 7 days prior to enrollment in this study) Antiplatelet agents and anticoagulants are not available; Have heparin, contrast agent and other allergies The subjects were participating in other uncompleted clinical trials Scheduled elective surgery Life expectancy is less than 1 year Patients with high blood risk Has long-term oral anticoagulant therapy adaptation Cardiogenic shock Patients with severe intraoperative dissection or hematoma requiring stent rescue
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Quan Guo, MD
    Phone
    +8615670510031
    Email
    xinyiguoquan@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Muwei Li, MD
    Organizational Affiliation
    Fuwai central China cardiovascular hospotial
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Rivaroxaban Combined With DAPT Versus DAPT Alone After Drug-coated Balloon Angioplasty

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