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Catheter Ablation of Ventricular Arrhythmia Reduces Skin Sympathetic Activity

Terminated
Conditions
Ventricular Tachycardia
Registration Number
NCT04837183
Lead Sponsor
Mayo Clinic
Brief Summary

This study is being done to determine whether there is an increase in sympathetic nerve activity before the onset of ventricular arrhythmias or irregular heartbeat rhythm. In addition, this study is looking at the relationship between sympathetic nerve activity and how patients with ventricular arrhythmias respond to catheter ablation treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patients who have non-sustained or sustained VA (VA ≥ 30s or receiving appropriate ICD therapies) are presented to the clinic or admitted to the hospital within 7 days of episodes.
  • The causes of VA are associated with structural heart diseases including ischemic or nonischemic cardiomyopathy (idiopathic cardiomyopathy, hypertrophic cardiomyopathy, cardiac sarcoidosis or amyloidosis, and arrhythmogentic right ventricular dysplasia).
  • Subjects are 18 years of age and older.
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Exclusion Criteria
  • Female patients who is pregnant or of childbearing potential and not on a reliable form of birth control.
  • Allergic to skin patch electrodes.
  • Vulnerable populations (fetuses, neonates, pregnant women, prisoners, institutionalized individuals).
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in LF/HF ratioBaseline, 24 hours post catheter ablation and approximately 3-6 months post-operative

low frequency (LF)/high frequency (HF) ratio of the skin sympathetic nerve activity

Change in amplitude of skin sympathetic nerve activityBaseline, 24 hours post catheter ablation and approximately 3-6 months post-operative

measured in µV

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mayo Clinic in Rochester

🇺🇸

Rochester, Minnesota, United States

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