Ventricular Tachycardia Clinical Trial
Official title:
Characterization of Cardiac Electrophysiological Effects of Autonomic Neuromodulation
Prospective cohort study evaluating the electrophysiologic and biochemical effects of stellate ganglion block in patients with ventricular tachycardia.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | July 1, 2027 |
Est. primary completion date | June 30, 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Planned catheter based VT ablation - Age at least 18 years Exclusion Criteria: - Pregnancy - Contraindication to SGB or VT ablation - Hypersensitivity of local anesthetic of amide type - Hemodynamic instability during the procedure prior to the study protocol |
Country | Name | City | State |
---|---|---|---|
United States | Hospital of the University of Pennsylvania | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pennsylvania |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ventricular Effective Refractory Period | Change in Ventricular Effective Refractory Period at 600ms drive train (measured in milliseconds) | 30 minutes following stellate ganglion block | |
Secondary | Ventricular Arrhythmia Inducibility | Induction of monomorphic ventricular arrhythmia (binary outcome) during ventricular programmed stimulation | 30 minutes following stellate ganglion block | |
Secondary | Neuropeptide Y | Change in level of neuropeptide Y from baseline (measured in pg/mL) | 30 minutes following stellate ganglion block |
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