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NCT05016921 Clinical Trial

TcMS to Treat Ventricular Tachycardia

Ventricular Tachycardia Clinical Trial

Official title:
Transcutaneous Magnetic Stimulation of the Stellate Ganglion to Treat Ventricular Tachycardia

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT05016921
Other study ID # 849193
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date January 1, 2024
Est. completion date January 1, 2024

Study information
Verified date April 2024
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Open label study of transcutaneous magnetic stimulation targeting the stellate ganglion in patients with ventricular tachycardia

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 1, 2024
Est. primary completion date January 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age >18years - Documented ventricular tachycardia within the preceding 72 hours Exclusion Criteria: - Pregnancy - Implanted ventricular assist device - Metal implanted in heard or neck (except the mouth) - Implanted medication pumps - Cochlear implant - Implanted brain stimulator - Ocular implant - History of malignancy in the region of stimulation (neck)

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• TcMS
Transcutaneous magnetic stimulation targeting the stellate ganglion

Locations
Country Name City State
United States Hospital of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Ventricular Tachycardia Burden (number of episodes) of ventricular tachycardia 0-72 hours after enrollment
Secondary Non sustained ventricular tachycardia Burden (number of episodes) of ventricular tachycardia 0-72 hours after enrollment
Secondary Discomfort Discomfort experienced during stimulation (on scale of 0-10) reported by patient Assessed immediately following stimulation
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