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Aspirin vs Clopidogrel After TAVR

Primary Purpose

Severe Aortic Stenosis

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Aspirin single antiplatelet therapy
Clopidogrel single antiplatelet therapy
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Aortic Stenosis

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients >19 years old
  2. Patients who underwent TAVR symptomatic severe AS
  3. Provision of informed consent

Exclusion Criteria:

  1. Patients requiring dual antiplatelet therapy longer than 4 weeks
  2. Any conditions requiring specific antiplatelet therapy aspirin or clopidogrel
  3. History of stroke or transient ischemic attack (TIA) within 6 months
  4. Planned major surgery
  5. Cardiogenic shock or hemodynamic instability
  6. Chronic kidney disease stage 4 or 5 (eGFR <30mL/min)
  7. Valve-in-valve TAVR procedure
  8. Hypersensitivity or contraindication to aspirin or clopidogrel
  9. Indication for anticoagulation therapy

Sites / Locations

  • Yonsei University Health System, Severance HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Aspirin group

Clopidogrel group

Arm Description

Patients receive the aspirin (100 mg/day) single antiplatelet therapy after 4 weeks of dual antiplatelet therapy of aspirin (100 mg/day) and clopidogrel (75 mg/day) after TAVR.

Patients receive the clopidogrel (75 mg/day) single antiplatelet therapy after 4 weeks of dual antiplatelet therapy of aspirin (100 mg/day) and clopidogrel (75 mg/day) after TAVR.

Outcomes

Primary Outcome Measures

Incidence of leaflet thrombosis
Incidence of leaflet thrombosis on cardiac CT at 3 months after TAVR

Secondary Outcome Measures

Any stroke
Ischemic Stroke
Transient ischemic attack
Thromboembolic events (composite of any stroke, myocardial infarction, systemic embolism (not involving the central nervous system), deep-vein thrombosis, or pulmonary embolism)
Echocardiographic parameters (maximum and mean aortic valve pressure gradient)
Echocardiographic parameters (doppler velocity index)
Echocardiographic parameters (paravalvular regurgitation)
Echocardiographic parameters (leaflet thrombosis)
VARC-3 type 3 or 4 bleeding
VARC-3 type 2 bleeding

Full Information

First Posted
August 8, 2022
Last Updated
October 10, 2023
Sponsor
Yonsei University
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1. Study Identification

Unique Protocol Identification Number
NCT05493657
Brief Title
Aspirin vs Clopidogrel After TAVR
Official Title
Aspirin Versus Clopidogrel for Leaflet Thrombosis Prevention in Patients Undergoing Transcatheter Aortic Valve Replacement: ACLO-TAVR Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 2, 2023 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yonsei University

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
Currently, the optimal antithrombotic therapy after transcatheter aortic valve replacement (TAVR) remains still unknown., The purpose of the study is to compare aspirin versus clopidogrel monoantiplatelet therapy for preventive effect on leaflet thrombosis in patients undergoing TAVR for severe aortic stenosis. This study is designed as a prospective, multicenter, open label, randomized controlled study. Eligible patients will be randomized to aspirin or clopidogrel monotherapy after TAVR. Patients will have dual antiplatelet therapy of aspirin 100 mg and clopidogrel 75 mg for 4 weeks after TAVR and then subsequent monoantiplatelet therapy of either aspirin 100 mg or clopidogrel 75 mg according to the randomization. Leaflet thrombosis will be assessed with cardiac computed tomography (CT) and transthoracic echocardiography at 3 months after TAVR. Patients will be clinically followed for 6 months. The primary endpoint is the Incidence of leaflet thrombosis on cardiac CT at 3 months.
Detailed Description
Prospective, multicenter, open label, randomized controlled study Eligible patients will be randomized to aspirin or clopidogrel monotherapy after TAVR All patients will have dual antiplatelet therapy of aspirin 100 mg and clopidogrel 75 mg for 4 weeks after TAVR and then subsequent monoantiplatelet therapy of either aspirin 100 mg or clopidogrel 75 mg. Leaflet thrombosis will be assessed with cardiac computed tomography (CT) and transthoracic echocardiography at 3 months after TAVR Clinical follow-up up to 6 months

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Aortic Stenosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
230 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Aspirin group
Arm Type
Active Comparator
Arm Description
Patients receive the aspirin (100 mg/day) single antiplatelet therapy after 4 weeks of dual antiplatelet therapy of aspirin (100 mg/day) and clopidogrel (75 mg/day) after TAVR.
Arm Title
Clopidogrel group
Arm Type
Experimental
Arm Description
Patients receive the clopidogrel (75 mg/day) single antiplatelet therapy after 4 weeks of dual antiplatelet therapy of aspirin (100 mg/day) and clopidogrel (75 mg/day) after TAVR.
Intervention Type
Drug
Intervention Name(s)
Aspirin single antiplatelet therapy
Intervention Description
Patients receive the aspirin (100 mg/day) single antiplatelet therapy after 4 weeks of dual antiplatelet therapy of aspirin (100 mg/day) and clopidogrel (75 mg/day) after TAVR.
Intervention Type
Drug
Intervention Name(s)
Clopidogrel single antiplatelet therapy
Intervention Description
Patients receive the clopidogrel (75 mg/day) single antiplatelet therapy after 4 weeks of dual antiplatelet therapy of aspirin (100 mg/day) and clopidogrel (75 mg/day) after TAVR.
Primary Outcome Measure Information:
Title
Incidence of leaflet thrombosis
Description
Incidence of leaflet thrombosis on cardiac CT at 3 months after TAVR
Time Frame
At 3 months after TAVR
Secondary Outcome Measure Information:
Title
Any stroke
Time Frame
3 months and 6 months after TAVR
Title
Ischemic Stroke
Time Frame
3 months and 6 months after TAVR
Title
Transient ischemic attack
Time Frame
3 months and 6 months after TAVR
Title
Thromboembolic events (composite of any stroke, myocardial infarction, systemic embolism (not involving the central nervous system), deep-vein thrombosis, or pulmonary embolism)
Time Frame
3 months and 6 months after TAVR
Title
Echocardiographic parameters (maximum and mean aortic valve pressure gradient)
Time Frame
at 3 months after TAVR
Title
Echocardiographic parameters (doppler velocity index)
Time Frame
at 3 months after TAVR
Title
Echocardiographic parameters (paravalvular regurgitation)
Time Frame
at 3 months after TAVR
Title
Echocardiographic parameters (leaflet thrombosis)
Time Frame
at 3 months after TAVR
Title
VARC-3 type 3 or 4 bleeding
Time Frame
3 months and 6 months after TAVR
Title
VARC-3 type 2 bleeding
Time Frame
3 months and 6 months after TAVR

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients >19 years old Patients who underwent TAVR symptomatic severe AS Provision of informed consent Exclusion Criteria: Patients requiring dual antiplatelet therapy longer than 4 weeks Any conditions requiring specific antiplatelet therapy aspirin or clopidogrel History of stroke or transient ischemic attack (TIA) within 6 months Planned major surgery Cardiogenic shock or hemodynamic instability Chronic kidney disease stage 4 or 5 (eGFR <30mL/min) Valve-in-valve TAVR procedure Hypersensitivity or contraindication to aspirin or clopidogrel Indication for anticoagulation therapy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Young-Guk Ko, MD, PhD
Phone
82-2-2228-8460
Email
ygko@yuhs.ac
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Young-Guk Ko, MD, PhD
Organizational Affiliation
Division of Cardiology, Yonsei Cardiovascular Hospital, Yonsei University College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Yonsei University Health System, Severance Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Young-Guk Ko, MD, PhD
Phone
82-2-2228-8460
Email
ygko@yuhs.ac

12. IPD Sharing Statement

Plan to Share IPD
No

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Aspirin vs Clopidogrel After TAVR

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