Intranasal Insulin for Posttraumatic Stress Disorder

Recruiting Phase 2 Interventional Study
PTSD
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
21 – 65
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
VA Connecticut Healthcare System · Federal
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About This Trial

To evaluate if intranasal insulin is effective in reducing PTSD symptoms.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Male or female, 21-65 years old * Current PTSD * Able to provide written informed consent Exclusion Criteria: * Unstable medical condition, clinically determined by a physician * Diabetes requiring insulin or oral hypoglycemic agents * Moderate-severe traumatic brain injury …
Contacts

Gihyun Yoon, MD

(203) 932-5711

gihyun.yoon@yale.edu

CONTACT