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NOT YET RECRUITING
NCT07561307
NA

Optimizing Stimulation Parameters for Electroconvulsive Therapy

Sponsor: University of Pennsylvania

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to improve how electroconvulsive therapy (ECT) stimulation settings are chosen. Researchers will use real-time brain monitoring to measure both seizures and a recently identified brain event called cortical spreading depolarization (CSD). The main questions it aims to answer are: What is the best way to increase ECT stimulation settings? How do different pulse settings affect the brain's response? Can certain settings produce CSD without causing a seizure? Participants already receiving ECT as part of their care will take part. They will be assigned to one of two groups: Index ECT group: Participants starting ECT will receive different standard titration approaches. Maintenance ECT group: Participants receiving ongoing ECT will undergo a brief, low-dose stimulation test before treatment. All participants will be monitored using brain physiology (EEG and blood flow) and symptom scales during treatment.

Official title: Parameter Refinement for ECT Stimulation and Titration Optimization

Key Details

Gender

All

Age Range

Any - Any

Study Type

INTERVENTIONAL

Enrollment

64

Start Date

2026-12-01

Completion Date

2030-06-30

Last Updated

2026-09-04

Healthy Volunteers

No

Interventions

PROCEDURE

Electroconvulsive Therapy

Electrical stimulation under anesthesia

Locations (1)

Pennsylvania Hospital

Philadelphia, Pennsylvania, United States