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RecruitingNCT07382596

Dextrose injection compared with saline for treatment-resistant PTSD

About this titleRead the official source — NCT07382596
Medication studyAges 19–90United States
The study in practice

Understand this study

Who could participate?

Listed age limits: 19 years to 90 years.

What will I do during this study?

You are randomly assigned to bilateral cervical plexus injections of dextrose solution or saline. The registry lists injections at weeks 0, 2, 4 and 8; from weeks 13 to 52, additional dextrose injections in the saline group are available on request. The record describes this as a comparison of injection approaches for people with PTSD.

Listed locations
Lexington and 3 more locationsSee all locations and recruitment
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Participation duration
Injections are listed at weeks 0, 2, 4 and 8, with requested injections possible from weeks 13–52.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: May 16, 2026
Recruitment status
Recruiting
Enrollment listed in the registry
50
Sponsor
Dr. Dean Reeves Clinic
Sponsor type
Individual investigator
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 19 Years to 90 Years
Official registry ID
NCT07382596
Official title
Show the full official title

Cervical Plexus Hydrodissection With D5W Versus NS for Treatment-Resistant PTSD

Recruitment & locations

Currently recruiting

Lexington · Portland · Madison

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Dr. Dean Reeves Clinic.

Does this study involve medication?

Yes. The study involves medication, including Dextrose 5% in water bilateral injection and Normal saline bilateral injection.

Who can participate?

Listed age limits: 19 years to 90 years.

Is this study still recruiting?

The registry lists this study as recruiting.

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