Ketamine for Depression in Veterans with Parkinson's Disease
This study is testing if ketamine can help Veterans with Parkinson's disease (PD) who also experience depression. Many people with PD struggle with depression, and current treatments don't always work well. Researchers are giving either ketamine or remimazolam (an active placebo) through an IV to 80 Veterans with PD. They want to see if ketamine improves depression symptoms within 24 hours. They are also looking at how ketamine might affect the brain's ability to adapt (neuroplasticity) and reduce inflammation, which are thought to be involved in PD. To join, you need to be a U.S. Veteran with PD, between 40 and 80 years old, and have not responded well to at least one antidepressant medication.
- Study design
- This is a double-masked, active placebo-controlled study, meaning neither you nor your doctor will know if you are receiving ketamine or remimazolam. About 80 Veterans with Parkinson's disease will participate.
- What's involved
- You would receive a single intravenous (IV) infusion of either ketamine or remimazolam. Clinical assessments for adverse events, tolerability, and depression will be conducted, along with non-invasive brain stimulation and blood tests.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your depression symptoms will be measured at baseline and 24 hours after the infusion.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Ketamine for Veterans With Parkinson's Disease
At a glance
Conditions
NCT06231563
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
San Francisco VA Medical Center, San Francisco, CA
San Francisco, Californiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Ellen R Bradley, MD · PRINCIPAL_INVESTIGATOR · San Francisco VA Medical Center, San Francisco, CA
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Montgomery-Asberg Depression Rating Scale (MADRS)baseline and 24 hours post-infusion.
Changes in depression as measured by the Montgomery-Asberg Depression Rating Scale (MADRS) between baseline and 24 hours post-infusion. Overall score ranges from 0 to 60, where higher scores indicate more severe depression