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SAINT in Postpartum Depression (PPD)

NCT07210255

This study is recruiting at 4 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

Summary

This study is a large, multi-site clinical trial testing whether Stanford Accelerated Intelligent Neuromodulation Therapy (SAINT), a fast-acting form of repetitive transcranial magnetic stimulation (rTMS), can more effectively reduce symptoms of postpartum depression (PPD) compared to a sham treatment. It will enroll 192 women within 12 months postpartum who are experiencing depression, and will track their progress for up to 12 months. The trial's main goal is to see if SAINT leads to reduction in depression severity in women with postpartum depression.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Postpartum Depression (PPD)

Eligibility basics and study details

Study type
Interventional
Phase
Not applicable
Ages
18 to 45 years
Sex
Female
Healthy volunteers
Not accepted
Sponsor
Magnus Medical
Last updated on ClinicalTrials.gov
September 28, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Massachusetts · 1

  • UMass Chan Medical School · Worcester, MA

New York · 1

  • Icahn School of Medicine at Mount Sinai · New York, NY

South Carolina · 1

  • The Medical University of South Carolina (MUSC) · Charleston, SC

Texas · 1

  • University of Texas at Austin, Dell Medical School, Health Discovery Building · Austin, TX

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.