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Catheter Ablation of Ventricular Arrhythmia Reduces Skin Sympathetic Activity

Catheter Ablation of Ventricular Arrhythmia Reduces Skin Sympathetic Activity

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04837183
Enrollment
30
Registered
2021-04-08
Start date
2021-11-15
Completion date
2024-01-01
Last updated
2024-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventricular Tachycardia

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.

Interventions

None listed

Sponsors

Cedars-Sinai Medical Center
CollaboratorOTHER
Mayo Clinic
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

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).

Design outcomes

Primary

MeasureTime frameDescription
Change in amplitude of skin sympathetic nerve activityBaseline, 24 hours post catheter ablation and approximately 3-6 months post-operativemeasured in µV
Change in LF/HF ratioBaseline, 24 hours post catheter ablation and approximately 3-6 months post-operativelow frequency (LF)/high frequency (HF) ratio of the skin sympathetic nerve activity

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026