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The Effect of Late Na Current Blocker Mexiletine on Giant T-wave Electrical Alternans(STOP-TWA)

Not Applicable
Recruiting
Conditions
Giant T-wave Electrical Alternans
Interventions
Other: Conventional therapy
Registration Number
NCT05619120
Lead Sponsor
First Affiliated Hospital Xi'an Jiaotong University
Brief Summary

The electrocardiogram is one of the most basic tests for cardiovascular disease. T wave alternans (TWA), which reflects abnormal ventricular repolarization, can easily trigger ventricular tachycardia (VT) and ventricular fibrillation (VF), which are important warning clues for sudden cardiac death (SCD). The late sodium current (INaL) is an important component of the frequency-dependent regulation of cardiac repolarization, and various causes of delayed repolarization can increase INaL. Our study on long QT syndrome (LQTS) found that INaL abnormalities can lead to abnormal myocardial repolarization, producing a giant TWA that triggers VT and VF. VT and VF, and INaL inhibition by the INaL blocker mexilate can terminate this process. This suggests that pharmacological blockade of INaL may be a potential target for the prevention of SCD by ameliorating the different causes of giant TWA and its triggering ventricular arrhythmic events. In this study, we propose to randomize patients with VT/VF triggered by giant TWA to conventional treatment and conventional treatment adds mexiletine treatment to compare the effects of the two treatment regimens on giant TWA and its triggered nonsustained VT, sustained VT, and VF; at the same time, we will compare the effects of mexiletine on giant TWA and its triggered ventricular arrhythmias of various etiologies by intra-group control before and after treatment. The safety and efficacy of the treatment of TWA and its triggered ventricular arrhythmias are compared.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Clinical diagnosis of macroscopic TWA
Exclusion Criteria
  • The patients who do not agree to participate in the study,
  • Patients with acute coronary syndrome or with progressive myocardial ischemia according to clinical manifestations, electrocardiogram or myocardial biochemical markers;
  • Those who have used other class I antiarrhythmic drugs or who are contraindicated by mexiletine.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Giant T-wave electrical alternans conventional therapyConventional therapyConventional treatment in the control group according to the guidelines for the management of ventricular arrhythmias (2017 AHA/ACC/HRS)
Giant T-wave electrical alternans conventional plus mexiletine therapyConventional therapyIt is proposed that patients presenting with giant TWA-triggered VT/VF patients to be randomized to conventional treatment and conventional plus mexiletine treatment, respectively.
Giant T-wave electrical alternans conventional plus mexiletine therapyMexiletineIt is proposed that patients presenting with giant TWA-triggered VT/VF patients to be randomized to conventional treatment and conventional plus mexiletine treatment, respectively.
Primary Outcome Measures
NameTimeMethod
Change in the occurrence of macroscopic TWAat administration,1,2,3,4,5,6,7 days after administration.

Macroscopic TWA occurring on conventional ECG (12-lead ECG, telemetry ECG, or holter ECG) with visually identifiable TWA Diagnosis confirmed by at least 3 leading ECG specialists. The data is obtained from the medical records.

Secondary Outcome Measures
NameTimeMethod
Change in the number of refractory casesAt administration,1,2,3,4,5,6,7 days after administration.

The number of cases in the group requiring ICD for ventricular arrhythmia episodes. The data is obtained from the medical records.

Length of hospital stayAbout 7 days after administration.

Comparison between two treatment groups due to the effect of ventricular arrhythmia episodes on the duration of hospitalization ( days) in patients. The data is obtained from the medical records.

Trial Locations

Locations (1)

First Affiliated Hospital of Xian Jiantong University

🇨🇳

Xi'an, Shaanxi, China

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