CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 62 enrolled
Drug / intervention
MECTA Spectrum 5000Q Amplitudedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02999269
NCT02999269Phase 4Completed

ECT Pulse Amplitude and Medial Temporal Lobe Engagement

University of New Mexico·interventional·Posted Dec 21, 2016·Updated Jul 24, 2023

In Brief

A Phase 4 clinical trial evaluating MECTA Spectrum 5000Q Amplitude for Major Depressive Disorder. Completed, enrolled 62 participants across 1 site.

Detailed Summary

Electroconvulsive therapy (ECT) remains the gold-standard treatment for patients with depressive episodes. During a typical four-week ECT series, most depressive episodes will respond to treatment and people will improve their level of functioning (return to work or family). Independent of the antidepressant effect of ECT, many patients experience transient memory impairment. This investigation will examine the impact of one ECT parameter (pulse amplitude or current) on brain changes (structure of connections within the brain) and clinical outcomes. The goal of this investigation is to determine the optimal parameter for an individual patient that will maintain the clinical response (reduce depression severity) and minimize side effects (eliminate memory issues related to treatment).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedDec 21, 2016
Enrollment StartOct 1, 2016
Primary CompletionMar 23, 2020
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 9.5 years ago

Interventions

MECTA Spectrum 5000Q Amplitudedevice

Current