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NCT Number: NCT07501819

Sympathetic Ablation for Ventricular Arrhythmias

Enrolled patients will undergo an acute procedure in which a catheter is inserted near the heart to ablate a sympathetic nerve, reducing signals that trigger ventricular arrhythmias.

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Key information

About this study

The autonomic nervous system controls cardiac activity, and sympathetic hyperactivity is an important factor in triggering and sustaining cardiac arrhythmias such as ventricular tachycardia (VT). The objective of this study is to evaluate a new treatment for VT that targets a specific nerve that is part of the sympathetic system. In an acute procedure, an ablation catheter will be inserted into the femoral artery and guided to locations near the heart. Radiofrequency energy will be delivered to ablate the neural targets, and the catheter will be removed. Patients will be subsequently followed to determine safety and post-ablation reduction in VT frequency.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 or older at the time of informed consent
  • Willing and capable of providing written informed consent
  • Implanted ICD or CRT-D
  • Recurrent VT leading to ICD therapy (ATP or shock)
  • Indicated for catheter ablation of VT per international guidelines
  • No prior instrumentation or resection of the stellate ganglia, or surgical procedure that may have disturbed the stellate ganglia

Exclusion criteria

  • Contraindication to percutaneous femoral arterial access
  • Heparin-induced thrombotic thrombocytopenia
  • Prior surgical sympathectomy
  • ECMO therapy in the past 30 days
  • Contraindicated for advanced heart failure therapies (LVAD or heart transplantation)
  • A most recently documented LVEF <20% in the past 30 days
  • Receiving inotropic drug therapy
  • Women of childbearing potential who are pregnant or breastfeeding. Women of childbearing potential must have a negative pregnancy test at enrollment
  • A life expectancy of less than 12 months according to physician judgment
  • Involvement in any concurrent clinical study with an investigational therapy

Treatment and study plan

Central sympathetic nerve ablation

Device

Catheter-based ablation of an extra-cardiac nerve target

Primary outcomes

  1. Freedom from device and procedure-related serious adverse events (SAEs)

    Time frame: 3 months

  2. VT burden (episodes per month)

    Time frame: 3 months

    VT burden post-ablation will be compared to VT burden pre-ablation

Study contacts

Contact information is provided by the study sponsor or research team.

Imad Libbus, PhD

CONTACT

[email protected]

651-242-4431

Sponsors and collaborators

Lead sponsor

SymKardia

Industry

Registry information

Official study title

Early Feasibility Study of Central Sympathetic Nerve Ablation for Treatment of Ventricular Arrhythmias

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Mar 30, 2026
Registry last updated
Mar 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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