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Comparative Study of Rosuvastatin/Ezetimib 20/10 mg and Atovastatin/Ezetimib 40/10 mg

Primary Purpose

Coronary Artery Disease, Dyslipidemias

Status
Recruiting
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
a high dose of statin/ezetimib
Sponsored by
Yonsei University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease

Eligibility Criteria

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

Inclusion Criteria: 19 years of age or older Patients who underwent a new generation of drug elution stent implantation for cardiovascular disease Exclusion Criteria: LDL cholesterol levels below 55 mg/dL without statin treatment Serum AST/ALT with an acute liver disease within a month or a normal upper limit that is not continuously explained Allergies or overreactions to statins Estimated Dawn of Less than 1 Year If it is determined that follow-up is not possible for more than one year Pregnancy

Sites / Locations

  • Yongin Severance HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

rosuvastatin/ezetimibe 20/10mg

atorvastatin/ezetimibe 40/10mg

Arm Description

rosuzet 10/20mg

NB zet 10/40mg

Outcomes

Primary Outcome Measures

Percentage of statins changed
Percentage of statins changed to discontinuation or intolerance (muscle pain, muscle efficiency, elevated liver level, etc.) within a year
Rate at which LDL cholesterol remains below 55 mg/dL
Rate at which LDL cholesterol remains below 55 mg/dL in all 1-year blood tests

Secondary Outcome Measures

The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
Cardiovascular death
Cardiovascular death
number of non-fatal myocardial infarction
number of non-fatal myocardial infarction
number of non-fatal stroke
number of non-fatal stroke
number of coronary artery re-perfusion
number of coronary artery re-perfusion
number of Newly developed diabetes or difficulty in controlling sugar
number of Newly developed diabetes or difficulty in controlling sugar
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
Increased muscle enzyme aberration
Increased muscle enzyme aberration (CPK > 4 x normal upper limit)
Elevated liver enzyme levels
Elevated liver enzyme levels (AST, ALT, or both ≥ 3 x normal upper bound)
Elevated serum creatine levels
Elevated serum creatine levels (from >50% baseline)
number of Major bleeding
number of Major bleeding
number of people who stopped taking the drug
number of people who stopped taking the drug

Full Information

First Posted
March 31, 2023
Last Updated
June 14, 2023
Sponsor
Yonsei University
Collaborators
dotter
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1. Study Identification

Unique Protocol Identification Number
NCT05910476
Brief Title
Comparative Study of Rosuvastatin/Ezetimib 20/10 mg and Atovastatin/Ezetimib 40/10 mg
Official Title
A Randomized comparaTive Study Of Rosuvastatin/Ezetimibe 20/10mg and Atorvastatin/Ezetimibe 40/10mg in Patients With Coronary Artery Drug eLuting stEnt Implantation Requiring High-dose stAtin/Ezetimibe combiNaTion Therapy: TOLERANT Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 3, 2023 (Actual)
Primary Completion Date
September 22, 2026 (Anticipated)
Study Completion Date
September 22, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Yonsei University
Collaborators
dotter

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
the investigators would like to compare the differences between roschvastin and atovastatin in patients who require high-dose statin/ejetimib to undergo a new generation of drug elution stent implantation for cardiovascular disease and maintain LDL cholesterol below 55 mg/dL.
Detailed Description
Death from vascular disease accounts for about one-third of all causes of death. Important regulatory factors in cardiovascular disease include dyslipidemia, high blood pressure, and diabetes, and keeping LDL cholesterol low among dyslipidemia levels, especially after cardiovascular stent treatment, is an essential factor to prevent another event in the future. Statin is currently the most widely used LDL cholesterol control drug with multifunctional effects such as controlling inflammatory reactions, controlling the movement and proliferation of vascular smooth muscle cells, and inhibiting the production of blood clots in addition to LDL cholesterol control.In addition, in several clinical studies, statins have shown many effects in primary and secondary prevention of cardiovascular disease, and several studies have been published that lower LDL cholesterol results in more benefits. Based on these findings, the 2016 European Heart Association (ESC), 2018 American Heart Association (ACC), and most recently changed 2022 Korean guidelines recommend controlling LDL cholesterol to <55mg/dL for patients with coronary artery disease. However, high-dose statins alone are still difficult to maintain for a long time due to increased liver levels, diabetes, and muscle pain, and recently, a drug that lowers LDL cholesterol has been developed in the small intestine called Ezetimib and is widely used in combination with statins in actual clinical trials. In fact, the RACING trial published in LANCET for domestic patients reported that the combination of moderate-intensity statins (Rosuvastatin 10mg) and ezetimib had fewer side effects for three years and better compliance, resulting in a better rate of maintaining LDL cholesterol at 70mg/dL or less than high-intensity statins alone. However, in this study, the rate at which LDL cholesterol remained below 55 mg/dL after one year was only 42% for moderate statins/esetimibe and 25% for high-intensity statins, and remained similar for three years. Therefore, high-intensity statins and ezetimibes may be essential treatments to reduce LDL cholesterol to less than 55 mg/dL and more than 50% under the current new guidelines. High-strength statins usually refer to more than 40 mg of atovastatin and 20 mg of Rosuvastatin, and drugs that combine ezetimibe with these high-strength statins are currently widely used to lower LDL cholesterol to 55 mg/dL or less if there are no special side effects in clinical practice, but research on compliance is very insufficient. This study aims to observe the rate of discontinuation or intolerance in patients taking Rosuvastatin/Ezetimib 20/10mg and Atovastatin/Ezetimib 40/10mg, with no previous comparison, RACING trial reported a 5% rate of discontinuation at rosuvastain 20mg administered, and atovatin/10mg/10mg. Referring to On the use of a pilot sample for sample size determination. the hospital conducts about 60 PCI cases a month, and about 1/5 of them are expected to be able to enroll 100 patients per group for about two years to conduct a total of 200 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Dyslipidemias

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
rosuvastatin/ezetimibe 20/10mg
Arm Type
Active Comparator
Arm Description
rosuzet 10/20mg
Arm Title
atorvastatin/ezetimibe 40/10mg
Arm Type
Active Comparator
Arm Description
NB zet 10/40mg
Intervention Type
Drug
Intervention Name(s)
a high dose of statin/ezetimib
Intervention Description
In randomization, 100 patients will proceed with Rosuvastatin/Ezetimib 20/10 mg and 100 patients will proceed with Atovastatin/Ezetimib 40/10 mg. A new generation of drug elution stents can be inserted and later registered, and if the patient agrees to participate in the study, they are randomly assigned after stent implantation.
Primary Outcome Measure Information:
Title
Percentage of statins changed
Description
Percentage of statins changed to discontinuation or intolerance (muscle pain, muscle efficiency, elevated liver level, etc.) within a year
Time Frame
12 months
Title
Rate at which LDL cholesterol remains below 55 mg/dL
Description
Rate at which LDL cholesterol remains below 55 mg/dL in all 1-year blood tests
Time Frame
12 months
Secondary Outcome Measure Information:
Title
The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
Description
The rate at which LDL cholesterol is maintained at 55 mg/dL in the blood test after a month
Time Frame
1 months
Title
Cardiovascular death
Description
Cardiovascular death
Time Frame
12 months
Title
number of non-fatal myocardial infarction
Description
number of non-fatal myocardial infarction
Time Frame
12 months
Title
number of non-fatal stroke
Description
number of non-fatal stroke
Time Frame
12 months
Title
number of coronary artery re-perfusion
Description
number of coronary artery re-perfusion
Time Frame
12 months
Title
number of Newly developed diabetes or difficulty in controlling sugar
Description
number of Newly developed diabetes or difficulty in controlling sugar
Time Frame
12 months
Title
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
Description
occurrence of statin-related muscle symptoms requiring therapeutic or dose changes
Time Frame
12 months
Title
Increased muscle enzyme aberration
Description
Increased muscle enzyme aberration (CPK > 4 x normal upper limit)
Time Frame
12 months
Title
Elevated liver enzyme levels
Description
Elevated liver enzyme levels (AST, ALT, or both ≥ 3 x normal upper bound)
Time Frame
12 months
Title
Elevated serum creatine levels
Description
Elevated serum creatine levels (from >50% baseline)
Time Frame
12 months
Title
number of Major bleeding
Description
number of Major bleeding
Time Frame
12 months
Title
number of people who stopped taking the drug
Description
number of people who stopped taking the drug
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 19 years of age or older Patients who underwent a new generation of drug elution stent implantation for cardiovascular disease Exclusion Criteria: LDL cholesterol levels below 55 mg/dL without statin treatment Serum AST/ALT with an acute liver disease within a month or a normal upper limit that is not continuously explained Allergies or overreactions to statins Estimated Dawn of Less than 1 Year If it is determined that follow-up is not possible for more than one year Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
deok kyu CHO, MD
Phone
+82-31-5189-8755
Email
CHODK123@yuhs.ac
First Name & Middle Initial & Last Name or Official Title & Degree
Yongcheol Kim, MD
Phone
+82-31-5189-8786
Email
decenthyun@yuhs.ac
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yongcheol Kim, MD
Organizational Affiliation
Yonsei University
Official's Role
Study Director
Facility Information:
Facility Name
Yongin Severance Hospital
City
Yongin
State/Province
Gyeonggi-do
ZIP/Postal Code
16995
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
deok kyu CHO, MD
Phone
+82-31-5189-8755
Email
CHODK123@yuhs.ac

12. IPD Sharing Statement

Learn more about this trial

Comparative Study of Rosuvastatin/Ezetimib 20/10 mg and Atovastatin/Ezetimib 40/10 mg

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