Neurosteroids for Treatment of PTSD in Veterans
Key facts
- Who runs it
- VA Office of Research and Development
- Where
- Durham, United StatesSee the site
- Trial code
- Status
- Completed
- Phase
- Phase 2
- People taking part
- 97 people enrolled
- Started
- 27 Jun 2019
- Ended
- 14 Jul 2025
- Type of study
- Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
- Treatments tested
- Pregnenolone
- Placebo
- Record updated
- 26 August 2026
Who can take part
- Age
- 18 years to 65 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 16 criteriaShow less
Who can take part
- At study outset: DSM-5 diagnosis of PTSD with CAPS-5 Total Score >=30. Following protocol amendment effective 4/13/2023: criterion modified to require diagnosis of PTSD using the CAPS-5 definition, defined by the following: at least one Criterion B symptom, at least one Criterion C symptom, at least 2 Criterion D symptoms and at least 2 Criterion E symptoms. This thus replaced the firm cutoff of CAPS-5 Total Score >=30
- Females will be required to use a medically and study approved contraceptive or otherwise not be of child-bearing potential; Birth control methods must be non-hormonal
- No anticipated need to alter psychiatric medications for duration of study involvement
- Ability to participate fully in the informed consent process
Who cannot take part
- Current suicidal or homicidal ideation necessitating clinical intervention or representing an imminent concern; Prior suicide attempt history or suicidal ideation that does not require clinical intervention or represent an imminent concern is permitted
- Standard pharmacological interventions for PTSD will not be exclusionary, including, but not limited to:; antidepressant medications such as SSRIs, SNRIs, tricyclics, bupropion, mirtazapine, venlafaxine, and nefazodone; mood stabilizers such as carbamazepine, divalproex, lamotrigine, topiramate; atypical antipsychotics, and other agents including prazosin; However, there may be no changes in psychotropic medications for PTSD 4 weeks prior to study randomization
- Initiation or change in psychotherapy within 3 months of randomization, i.e. psychotherapy must be stable for 3 months prior to study start
- Participants on hormonal therapies such as finasteride or hormonal birth control
- History of allergy to pregnenolone
- Medical disorders that may preclude safe administration of pregnenolone or exacerbate PTSD symptoms
- Serious unstable medical illness, such as:; history of cerebrovascular accident; prostate, uterine, or breast cancer; others (at the discretion of the PI and medical oversight team)
- Medical conditions not well controlled will be excluded, at the discretion of the PI and Medical Team
- Current diagnosis of bipolar disorder, schizophrenia or other psychotic disorder, or cognitive disorder due to a general medical condition other than mild TBI (assessed at screening)
- As indicated by the DSM-5, moderate or severe Substance Use Disorders (excluding caffeine and tobacco) within 1 month of study entry; Mild Alcohol Use Disorder is not exclusionary, at the judgment of the PI and her medical team
- Benzodiazepine use
- Female participants who are pregnant or breast-feeding
Where in United States
- Durham VA Medical Center, Durham, NCDurham, United States
About the trial
What the trial wants to find out
This study seeks to determine if pregnenolone can improve symptoms of PTSD and other symptoms that commonly occur with PTSD in Iraq/Afghanistan-era Veterans. The total study duration for each participant is 10 weeks. Eligible Veterans with PTSD will receive either pregnenolone or placebo throughout the study duration and will complete mental and physical health assessments at each study visit. Eligible participants will attend 6 in-person study visits and receive several short "check-in" phone calls.
The 2 groups in the trial
- PregnenoloneTreatment being tested
Placebo lead in 14 DAYS, followed by Pregnenolone 50 mg BID x 14 DAYS, followed by Pregnenolone 150 mg BID x 14 DAYS, followed by Pregnenolone 250 mg BID x thereafter for the remainder of the 8-week trial
- PlaceboPlacebo, for comparison
Matching placebo medication dispensed identically with the same number and frequency as the experimental arm
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Neurosteroid Intervention for PTSD in Iraq/Afghanistan-era Veterans
- Record updated
- 26 August 2026