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Clinical trialNCT07210255RecruitingInterventional

SAINT in Postpartum Depression (PPD)

SponsorMagnus MedicalEnrollment192Postpartum Depression (PPD)
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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 that has not improved with standard care, 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.

Investigators

No overall officials are registered on this study record. Site-level investigators, where published, appear with their sites below. Why? →

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

4 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Umass Chan Medical School

    Worcester, Massachusetts, United States

    Kimberly Yonkers, MD
    Recruiting
  • Icahn School of Medicine at Mount Sinai

    New York, New York, United States

    Thalia Robakis, MD, PhDVeerle Bergink, MD, PhD
    Recruiting
  • the Medical University of South Carolina (musc)

    Charleston, South Carolina, United States

    Connie Guille, MD
    Recruiting
  • University of Texas at Austin, Dell Medical School, Health Discovery Building

    Austin, Texas, United States

    Jeffrey Newport, MD, MS, MDiv
    Recruiting

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
1 Nov 2025
Primary completion
30 Apr 2029
Completion
31 Oct 2029
Last update posted
14 May 2026
Registered enrollment
192
Registry id
NCT07210255

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.