Loading
Life sciences · Phase 2/3 Trial
ClinicalTrials.gov · September 29, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Phase 2/3 Trial.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
This record has not been graded across any dimension yet. Treat the label above as provisional and read the source.
What is missing. This record has no bottom line, key findings, reported figures, evidence dimensions. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT05054699). This is a study registration, not published results. Lead sponsor: University of Sao Paulo. Recruitment status: COMPLETED. Phase: PHASE2, PHASE3. Study type: INTERVENTIONAL. Enrollment: 100 participants (ACTUAL). Conditions: Major Depressive Disorder, Bipolar Depression. Interventions: DEVICE: Magnetic Seizure Therapy; DEVICE: Electroconvulsive Therapy. Primary outcome measures: Depressive symptoms , Change from baseline to endpoint (week 18). However, the endpoint can be at week 12 if the patient is remitted at this time period.; Biographical memory , Change from baseline to endpoint (week 18). However, the endpoint can be at week 12 if the patient is remitted at this time period.. Brief summary: This study aims to compare the efficacy and safety profile of Magnetic Seizure Therapy and Electroconvulsive therapy.