Search | Clinical Trials Finder

These results were retrieved from the live ClinicalTrials.gov registry. Filters and sort order apply to this result list.

ClinicalTrials.gov public records Last synced Nov 6, 2026, 12:41 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Showing 1–24 of 33 matching trials from the live ClinicalTrials.gov search.

Filters: Condition: Postpartum Depression (PPD) Clear all

Conditions: Postpartum Depression
Interventions: WB001, ED001; Device
Lead sponsor: Woebot Health; Industry
Eligibility: 22 Years to 45 Years · Female only
Enrollment: 7 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2022 – 2023
U.S. locations: 8
States / cities: Lafayette, California • Santa Ana, California • DeLand, Florida + 5 more

Conditions: Depression, Postpartum, Postpartum Depression (PPD), Post-partum Depression, Postnatal Depression, Post-Natal Depression, Peripartum Depression
Interventions: LPCN 1154A, Placebo; Drug
Lead sponsor: Lipocine Inc.; Industry
Eligibility: 15 Years to 45 Years · Female only
Enrollment: 120 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2026 – 2027
U.S. locations: 16
States / cities: Tucson, Arizona • Canoga Park, California • Walnut Creek, California + 13 more

Conditions: Postpartum Depression (PPD), Postpartum Anxiety
Interventions: Not listed
Lead sponsor: University of Hawaii; Other
Eligibility: 18 Years and older · Female only
Enrollment: 100 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2026 – 2027
U.S. locations: 1
States / cities: Honolulu, Hawaii

Conditions: Postpartum Depression
Interventions: ROSE (Reach Out, Stay Strong, Essentials for mothers of newborns), Enhanced Care as Usual (CAU); Behavioral
Lead sponsor: Michigan State University; Other
Eligibility: 18 Years and older · Female only
Enrollment: 2,320 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2023 – 2027
U.S. locations: 1
States / cities: Flint, Michigan

Conditions: Insomnia, Post Partum Depression
Interventions: dCBTI, Sleep Education; Behavioral
Lead sponsor: Henry Ford Health System; Other
Eligibility: 18 Years and older · Female only
Enrollment: 91 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2018 – 2019
U.S. locations: 1
States / cities: Novi, Michigan

Conditions: Postpartum Depression (PPD), Self-Efficacy, Parental Anxiety, Engagement, Patient, Usability, Length of Stay
Interventions: VoiceLove mobile phone application; Device
Lead sponsor: Vanderbilt University Medical Center; Other
Eligibility: 18 Years and older · Female only
Enrollment: 150 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2026 – 2028
U.S. locations: 1
States / cities: Nashville, Tennessee

Conditions: Depression, Postpartum
Interventions: SAGE-217, Placebo; Drug
Lead sponsor: Biogen; Industry
Eligibility: 18 Years to 45 Years · Female only
Enrollment: 200 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2020 – 2022
U.S. locations: 68
States / cities: Scottsdale, Arizona • Bentonville, Arkansas • Anaheim, California + 62 more

Conditions: Perinatal Depression, Postpartum Depression (PPD)
Interventions: Parents and Babies Virtual Group Intervention, Parents and Babies Hybrid Group Intervention; Behavioral
Lead sponsor: Northwestern University; Other
Eligibility: 18 Years and older · Female only
Enrollment: 16 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2026 – 2027
U.S. locations: 1
States / cities: Chicago, Illinois

Conditions: Postpartum Depression (PPD)
Interventions: Light therapy; Device
Lead sponsor: University of Michigan; Other
Eligibility: 18 Years and older · Female only
Enrollment: 30 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2026 – 2027
U.S. locations: 1
States / cities: Ann Arbor, Michigan

Conditions: Depression, Depressive Disorder, Depression, Postpartum, Behavioral Symptoms, Mood Disorders, Mental Disorders, Puerperal Disorders, Pregnancy Complications, Postpartum, PPD
Interventions: Ganaxolone, Placebo; Drug
Lead sponsor: Marinus Pharmaceuticals; Industry
Eligibility: 18 Years to 45 Years · Female only
Enrollment: 91 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2017 – 2020
U.S. locations: 16
States / cities: Little Rock, Arkansas • Costa Mesa, California • Lemon Grove, California + 13 more

Conditions: PostPartum Depression
Interventions: MamaLift Plus, Digital Sham App; Device
Lead sponsor: Healthcare Innovation Technology Lab; Industry
Eligibility: 18 Years to 50 Years · Female only
Enrollment: 142 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2023
U.S. locations: 1
States / cities: New York, New York

Conditions: Postpartum Depression
Interventions: RE104 for Injection; Drug
Lead sponsor: Reunion Neuroscience Inc; Industry
Eligibility: 18 Years to 45 Years · Female only
Enrollment: 84 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024 – 2025
U.S. locations: 38
States / cities: Birmingham, Alabama • Tucson, Arizona • Santa Monica, California + 31 more

Conditions: Post-partum Depression
Interventions: Stella (TM) Mobile Application; Device
Lead sponsor: Curio Digital Therapeutics, Inc.; Industry
Eligibility: 18 Years to 50 Years · Female only
Enrollment: 65 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2021
U.S. locations: 1
States / cities: New York, New York

Conditions: Postpartum Depression (PPD), Pregnancy
Interventions: Enlighten; Diagnostic Test
Lead sponsor: University of Virginia; Other
Eligibility: 18 Years and older · Female only
Enrollment: 500 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2025 – 2028
U.S. locations: 2
States / cities: Charlottesville, Virginia • Falls Church, Virginia

Conditions: Postpartum Depression
Interventions: Escitalopram (Lexapro); Drug
Lead sponsor: University of Rochester; Other
Eligibility: 18 Years and older · Female only
Enrollment: 20 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2004 – 2007
U.S. locations: 1
States / cities: Rochester, New York

Conditions: Postpartum Depression (PPD)
Interventions: SAINT Neuromodulation System, Sham SAINT Stimulation; Device
Lead sponsor: Magnus Medical; Industry
Eligibility: 18 Years to 45 Years · Female only
Enrollment: 192 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2025 – 2029
U.S. locations: 4
States / cities: Worcester, Massachusetts • New York, New York • Charleston, South Carolina + 1 more

Conditions: Severe Postpartum Depression
Interventions: BRII-296, Depo Medrol; Drug
Lead sponsor: Brii Biosciences Limited; Industry
Eligibility: 18 Years to 45 Years
Enrollment: 11 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2023 – 2024
U.S. locations: 11
States / cities: Sherman Oaks, California • Torrance, California • Boynton Beach, Florida + 7 more

Conditions: Post Partum Depression
Interventions: Standard of Care (SOC), SOC with Psychology Therapy (CBT); Behavioral
Lead sponsor: Michelle Lopez; Other
Eligibility: 18 Years and older · Female only
Enrollment: 545 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2019 – 2020
U.S. locations: 2
States / cities: Houston, Texas

Conditions: Postpartum Depression, Depression
Interventions: Not listed
Lead sponsor: National Institute of Mental Health (NIMH); NIH
Eligibility: 20 Years to 45 Years · Female only
Enrollment: 68 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2003 – 2017
U.S. locations: 1
States / cities: Bethesda, Maryland

Conditions: Postpartum Depression (PPD), Pregnancy
Interventions: Diagnostic Test: Enlighten; Device
Lead sponsor: University of Virginia; Other
Eligibility: 18 Years and older · Female only
Enrollment: 1,000 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2025 – 2030
U.S. locations: 1
States / cities: Charlottesville, Virginia

Conditions: Postpartum, Postpartum Depression (PPD), Hypertension Disorders in Pregnancy, Postpartum Anxiety, Postpartum Care, Care Coordination, Care Gaps
Interventions: Postpartum Doula Support in the NICU; Behavioral
Lead sponsor: Children's Hospital of Philadelphia; Other
Eligibility: 18 Years and older · Female only
Enrollment: 756 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2027 – 2031
U.S. locations: 14
States / cities: Newark, Delaware • Voorhees Township, New Jersey • Bryn Mawr, Pennsylvania + 9 more

Conditions: Postpartum Depression
Interventions: Use of internet based social marketing intervention, No use of social media; Other
Lead sponsor: University of Louisville; Other
Eligibility: 13 Years to 21 Years · Female only
Enrollment: 287 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2013 – 2015
U.S. locations: 8
States / cities: Carrollton, Kentucky • Covington, Kentucky • Elizabethtown, Kentucky + 5 more

Conditions: Postpartum Depression (PPD), Cardiac Event
Interventions: LHMoms Intervention, No intervention; Behavioral · Other
Lead sponsor: Columbia University; Other
Eligibility: 18 Years and older · Female only
Enrollment: 21 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2025 – 2030
U.S. locations: 4
States / cities: Brooklyn, New York • Jamaica, New York • New York, New York

Conditions: Depression, Postpartum, Depression, Post-Partum, Postpartum Depression (PPD), Post-Natal Depression, Peripartum Depression, Postnatal Depression
Interventions: LPCN 1154A, Placebo; Drug
Lead sponsor: Lipocine Inc.; Industry
Eligibility: 15 Years to 45 Years · Female only
Enrollment: 90 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2025 – 2026
U.S. locations: 18
States / cities: Anahiem, California • Canoga Park, California • Miami, Florida + 14 more

Search by objective public record fields.

[Study Evaluating the Efficacy and Safety of a Digital Therapeutic as an Adjunct to TAU in Postpartum Depression]

Brexanolone Lifting Outcomes Of Moms

AI-Enabled Wearable Monitoring for Detection of Postpartum Depression and Anxiety

The ROSE Scale-up Study: Informing a Decision About ROSE as Universal PPD Prevention

Insomnia and Rumination in Late Pregnancy and the Risk for Postpartum Depression

NICU Utilization of Remote Voice Technology to Improve mateRnal Experience (NURTURE)

A Study to Evaluate the Efficacy and Safety of SAGE-217 in Participants With Severe Postpartum Depression (PPD)

Parents and Babies Pilot

Informing Implementation of a Circadian-Focused Intervention for Postpartum Depression

A Clinical Trial of Intravenous (IV) Ganaxolone in Women With Postpartum Depression

Curio Digital Therapy for the Treatment of Post-partum Depression

RE104 Safety and Efficacy Study in Postpartum Depression

Mobile Application in the Management of Mild to Moderate Postpartum Depression (PPD)

Clinical Validation of a Predictive Test for Postpartum Depression

Lexapro in the Treatment of Patients With Postpartum Depression

SAINT in Postpartum Depression (PPD)

A Study of BRII-296 in Adults With Severe Postpartum Depression (PPD)

Maternal Mental Health in the Hospital Setting

Screening Evaluation for Women With Postpartum Depression

A Study of a Test for Postpartum Depression at Home

Postpartum Care in the NICU Multi-Site

Social Media, Teen Moms and PPD

Living Healthy for Moms RCT

A Study to Assess the Safety and Efficacy of Oral LPCN 1154A in Women With Severe PPD