Could a nasal spray of insulin help PTSD?
NCT ID NCT04044534
First seen Jun 26, 2026 · Last updated Jul 14, 2026 · Updated 2 times
Summary
This study tests whether a daily nasal spray of insulin can reduce PTSD symptoms. Twenty adults with current PTSD will receive either insulin or a placebo for several weeks. Researchers will measure symptom changes using a standard PTSD scale.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- intranasal insulin
- What this could lead to
- If it works, this could point toward a new way to ease PTSD symptoms using a familiar drug.
- What could go wrong
- This is a very small early-phase trial with only 20 people, so results may not apply widely. Insulin can cause low blood sugar or nasal irritation.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
10 people
The number who actually took part.
- Started
-
Oct 2024
- Finished
-
May 2026
- Lead sponsor
-
A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
21 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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 * Current psychotic disorder, bipolar disorder, cognitive disorder in the past 12 months * Current substance use disorders (except alcohol, tobacco, or cannabis) in the past 3 months * Changes in doses of psychotropic medications in the past 4 weeks * Initiation of individual therapy or counseling in the past 4 weeks * Imminent suicidal or homicidal risk * Contraindication to Insulin * History of claustrophobia * Presence of cardiac pacemaker or other electronic device or ferromagnetic metal foreign bodies in vulnerable positions as assessed by a standard pre-MRI safety screening questionnaire
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
VA Connecticut Healthcare System
West Haven, Connecticut, 06516, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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