Effects of Carvedilol on Suppressing the Premature Ventricular Complex/Ventricular Tachycardia From Outflow Tract

NCT ID: NCT03587558

Last Updated: 2018-07-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

104 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-05

Study Completion Date

2020-12-31

Brief Summary

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Carvedilol is known to be effective in reducing ventricular arrhythmias and mortality in patients with heart failure. It is suggested that one of the mechanisms is its ability to block store overload-induced Calcium release which activates spontaneous calcium release by Ryanodine receptors. Ventricular outflow tract tachyarrhythmia is known to be associated with calcium overload due to activation of Ryanodine receptors. The aim of this study is to evaluate the efficacy of Carvedilol on premature ventricular complex(PVC)/ventricular tachycardia(VT) originating from outflow tract.

Detailed Description

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Carvedilol is one of the third-generation beta-blockers effective in reducing ventricular arrhythmias and mortality in patients with heart failure. Antioxidative and alpha - blocking effects, along with nonselective beta - blockade, have been described as a mechanism of effect in various diseases.

The antiarrhythmic effect of carvedilol inhibiting atrial fibrillation or ventricular arrhythmia has been reported, but its mechanism is not yet clear. Among them, inhibition of store overload-induced Ca2+ release (SOICR) is suggested as an antiarrhythmic mechanism of carvedilol.

Stimulation of the beta receptor leads to the entry of calcium into the sarcoplasmic reticulum (SR) by opening the L-type calcium channel. The influx of calcium through the L-type calcium channel also increases the calcium release through the Ryanodine receptor (RyR) in the sarcoplasmic reticulum. This is called Ca-induced Ca release and is known as a normal physiological response. However, when calcium overload in the myofibrillar body occurs, spontaneous calcium release, known as SOICR, can occur through RyR, which can make triggered activity by inducing Na+/Ca2+ exchanger present in myocardium, leading to severe arrhythmia. Among several beta-blockers, only carvedilol has been known as a drug that can directly inhibit SOICR in combination with beta-blockade effect.

Ventricular tachyarrhythmia originating from the ventricular outflow tract is an arrhythmia occurring in a patient with normal cardiac function. The mechanism of the arrhythmia is known to be triggered activity which is caused by activation of RyR due to increased cyclic adenosine monophasphate, resulting in calcium overload, eventually causing activation of Na+/Ca2+ exchanger. The aim of this study is to evaluate the efficacy of Carvedilol on PVC/VT originating from outflow tract.

Conditions

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Ventricular Premature Complexes Outflow Tract Carvedilol

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Carvedilol group

Patients in this group are taking carvedilol to inhibit outflow tract PVC/VT. Dilatrend® sustained release form of Chong Kun Dang Pharmaceutical will be used (initial dose: 8 mg sustained release form). Outpatient follow-up will be performed every 2 weeks and the dose is increased from the initial dose to a maximal tolerable dose, at the discretion of the investigator.

Group Type EXPERIMENTAL

Carvedilol

Intervention Type DRUG

Patients in this group are taking carvedilol to inhibit outflow tract PVC/VT.

Flecainide group

Patients in this group are taking flecainide to inhibit outflow tract PVC/VT. Tambocor® of JW Pharmaceutical will be used. Outpatient follow-up will be performed every 2 weeks and the dose is increased from the initial dose to a maximal tolerable dose, at the discretion of the investigator.

Group Type ACTIVE_COMPARATOR

Flecainide

Intervention Type DRUG

Patients in this group are taking flecainide to inhibit outflow tract PVC/VT.

Interventions

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Carvedilol

Patients in this group are taking carvedilol to inhibit outflow tract PVC/VT.

Intervention Type DRUG

Flecainide

Patients in this group are taking flecainide to inhibit outflow tract PVC/VT.

Intervention Type DRUG

Other Intervention Names

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Dilatrend Tambocor

Eligibility Criteria

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Inclusion Criteria

* Patients with ventricular premature complexes/ventricular tachycardias originating from ventricular outflow tract confirmed on the 12-lead surface ECG
* Patients with PVC burden of 5% or more in 24-hour Holter monitoring
* Patients with normal left ventricular function

* left ventricular ejection fraction ≥50%
* Patients without structural heart disease

Exclusion Criteria

* Pregnant, trying to become pregnant or breast feeding
* History of bronchial asthma
* History of coronary arterial disease
Minimum Eligible Age

19 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Chong Kun Dang Pharmaceutical Corp.

INDUSTRY

Sponsor Role collaborator

Keimyung University Dongsan Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Seongwook Han, M.D., Ph.D.

Role: STUDY_CHAIR

Keimyung University Dongsan Medical Center

Locations

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Keimyung University Dongsan Medical Center

Daegu, , South Korea

Site Status RECRUITING

Division of Cardiology, Department of Internal Medicine, Kyungpook National University Hospital

Daegu, , South Korea

Site Status RECRUITING

Division of Cardiology, Department of Internal Medicine, Yeungnam University Hospital

Daegu, , South Korea

Site Status RECRUITING

Division of Cardiology, Department of Internal Medicine, Daegu Catholic University Medical Center

Daegu, , South Korea

Site Status RECRUITING

Chonnam National University Hospital

Gwangju, , South Korea

Site Status RECRUITING

Korea University Anam Hospital

Seoul, , South Korea

Site Status RECRUITING

Seoul National University Hospital

Seoul, , South Korea

Site Status RECRUITING

Severance Cardiovascular Hospital

Seoul, , South Korea

Site Status RECRUITING

Seoul Asan Medical Center

Seoul, , South Korea

Site Status RECRUITING

Seoul Samsung Medical Center

Seoul, , South Korea

Site Status RECRUITING

Seoul St. Mary's Hospital

Seoul, , South Korea

Site Status RECRUITING

Countries

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South Korea

Central Contacts

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Jongmin Hwang, M.D., Ph.D.

Role: CONTACT

+82-53-250-7333

Facility Contacts

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Jongmin Hwang, M.D.

Role: primary

+82-53-250-7333

Myung Hwan Bae, MD, PhD

Role: primary

Dong Gu Shin, MD, PhD

Role: primary

Young Soo Lee, MD, PhD

Role: primary

Hyung Wook Park, MD, PhD

Role: primary

Jong-Il Choi, MD, PhD

Role: primary

Eue-Keun Choi, MD, PhD

Role: primary

Boyoung Joung, MD, PhD

Role: primary

Jun Kim, MD, PhD

Role: primary

Young Keun On, MD, PhD

Role: primary

Sung-Hwan Kim

Role: primary

Other Identifiers

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2017-07-022

Identifier Type: -

Identifier Source: org_study_id

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