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NCT05699226

Amplitude Titration to Improve ECT Clinical Outcomes

Recruiting now NA Last updated 26 January 2026
What this trial tests

NA trial testing Soterix Medical Incorporated 4x1 adapter in Depression in 50 participants. Currently enrolling.

Timeline
14 September 2023
Primary endpoint
1 January 2027
1 January 2028

Quick facts

Lead sponsorUniversity of New Mexico
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment50
Start date14 September 2023
Primary completion1 January 2027
Estimated completion1 January 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of New Mexico

Who can join

50 and older, any sex, with Depression or ECT. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A randomized controlled trial will compare hippocampal neuroplasticity, antidepressant, and cognitive outcomes between individualized amplitude and fixed 800 mA amplitude ECT in older depressed subjects (n = 25 per group, n = 50 total). Relative to fixed 800 mA ECT: H1: Individualized amplitude arm will have improved RUL antidepressant outcome (IDS-C30 response rates and reduced BT electrode placement switch at V2). H2: Individualized amplitude arm will have improved cognitive outcomes (DKEFS-Verbal Fluency

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Depression

Currently open trials in the same condition.

Other University of New Mexico trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05699226.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing