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Study identifier: NCT06238700 Synced from ClinicalTrials.gov · August 05, 2026
● Recruiting

Study on Allopregnanolone and Depression in Women Across the Menopause Transition

Condition: Depression  ·  Sponsor: Beth Israel Deaconess Medical Center

PhaseNA
Planned participants80
Who can joinFemale, 40 Years to 60 Years
Healthy volunteersNo

About this study

This study aims to identify how enhanced allopregnanolone activity (via pregnenolone) affects behavior and neurobiology that may underlie perimenopausal depression.

This description comes directly from the study's public registry record.

Talk to the study team

Aleta Wiley, MPH  ·  617-975-8706  ·  awiley3@bidmc.harvard.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Beth Israel Deaconess Medical CenterBoston, Massachusetts, United StatesRecruiting

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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06238700