Recruiting
Study on Allopregnanolone and Depression in Women Across the Menopause Transition
This study aims to identify how enhanced allopregnanolone activity (via pregnenolone) affects behavior and neurobiology that may underlie perimenopausal depression.
ClinicalTrials.gov IDNCT06238700
PhaseNA
Enrollment80
SponsorBeth Israel Deaconess Medical Center
Age40 Years
SexFEMALE
Conditions studied
Depression
About this study
This study aims to identify how enhanced allopregnanolone activity (via pregnenolone) affects behavior and neurobiology that may underlie perimenopausal depression.
Interventions
- Dietary Supplement: pregnenolone — Pregnenolone is an endogenous steroid available in the US and elsewhere as an orally administered over-the-counter supplement.
- Other: placebo — Placebo pills are identical-appearing capsules containing cellulose
Primary outcomes
- Within-person change in score on the Ruminative Responses Scale (Baseline to 2 weeks)
Eligibility information
Inclusion Criteria:
* Healthy women ages 40 to 60 years in the menopause transition
* Depressive symptoms
* Psychotropic medications are allowed if the dose is stable prior to screening and throughout the study
* Able to read Arabic numerals and perform simple arithmetic
* Able to provide written informed consent
Exclusion Criteria:
* Systemic hormone therapy
* Contraindicated medications with pregnenolone
* Systemic corticosteroid
* Other psychiatric illnesses that are considered to be primary
* Current suicidal ideation
* Active substance use disorders
* Unstable medical conditions
* Obstructive sleep apnea or other primary sleep disorders
* Abnormal hepatic and renal function
* Known allergy to progesterone, exogenous allopregnanolone, or pregnenolone
* History of head injury resulting in loss of consciousness \> 20 min
* Inability to comply with barrier contraceptive methods
* Known intellectual disability
* Investigator judgement that study participation constitutes substantial risk given medical or psychiatric condition
* Current or recent participation in clinical trial expected to interfere with risk of or interpretation of study data
* Inability to comply with study procedures
Study locations
- Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215 United States
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.