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RecruitingNCT07473648

Multimodal Clinical Study of Electroconvulsive Therapy and Magnetic Seizure Therapy

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
The Second Hospital of Anhui Medical University · Academic / Other
Sex
All
Age
12 Years – 80 Years
Healthy volunteers
Accepted

Summary

To compare the efficacy and tolerability of Electroconvulsive Therapy (ECT) and Magnetic Seizure Therapy (MST) in patients with major depressive disorder (MDD).

Conditions

Interventions

TypeNameDescription
DEVICEElectroconvulsive TherapyElectroconvulsive therapy will be administered two to four times a week according to a standardized protocol. Stimulation parameters (including intensity, target location, session number, and duration) will be individualized for each participant based on prior research to ensure targeted and safe delivery within established safety limits. Treatment will continue until the participant meets the protocol-defined response criteria or completes a maximum of 10 sessions.
DEVICEMagnetic Seizure TherapyMagnetic seizure therapy will be administered two to four times a week according to a standardized protocol. Stimulation parameters (including intensity, target location, session number, and duration) will be individualized for each participant based on prior research to ensure targeted and safe delivery within established safety limits. Treatment will continue until the participant meets the protocol-defined response criteria or completes a maximum of 10 sessions.
OTHERCognitive and Behavioral AssessmentParticipants will undergo a series of standardized cognitive tests (e.g., MCCB) and behavioral assessments (e.g., clinical rating scales) at specified time points. This does not constitute a therapeutic intervention but is for the purpose of data collection to establish normative baseline performance.

Timeline

Start date
2025-09-01
Primary completion
2027-12-01
Completion
2028-01-01
First posted
2026-03-16
Last updated
2026-03-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07473648. Inclusion in this directory is not an endorsement.