EligibleTrials

Study on Allopregnanolone and Depression in Women Across the Menopause Transition

Recruiting · NCT06238700 · Interventional (participants receive a specific treatment) · Lead sponsor: Beth Israel Deaconess Medical Center

View the official record on ClinicalTrials.gov →
Depression

Interventions studied

placebopregnenolone

What this trial is about

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

Who can take part

Age range
40 Years to 60 Years
Sex
Female
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

1 location listed across 1 US state.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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