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Cervical Plexus Hydrodissection With D5W for PTSD
NCT04421573 · View on ClinicalTrials.gov ↗
Study Summary
PTSD is a chronic mental health condition that drastically reduces an individual's quality of life Dextrose injection with a small needle has been used for chronic pain patients and observational results have shown it to be effective in reducing anxiety, brain fog, and depression in patients with PTSD. This randomized trial will compare dextrose injection with a delayed/usual treatment control.
Conditions Studied
Interventions
- PROCEDURE BCPHD with D5W
- PROCEDURE Waiting period with usual care
Study Locations (4)
Oregon
- Paul W. Johnson, D.O., Clinic. — Portland
- NW Regen — Tigard
Kentucky
- Danesh Mazloomdoost — Lexington
Wisconsin
- Eric Phillippi M.D. Clinic — Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2023-07-10 |
| Est. Completion | 2027-10-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04421573
The ClinicalTrials.gov registry entry for NCT04421573 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dr. Dean Reeves Clinic, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with PTSD appearing as the primary indexed condition, and to 2 interventions — of which BCPHD with D5W is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04421573 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Oregon, Kentucky, Wisconsin. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04421573 about?
NCT04421573 is a clinical study titled "Cervical Plexus Hydrodissection With D5W for PTSD". PTSD is a chronic mental health condition that drastically reduces an individual's quality of life Dextrose injection with a small needle has been used for chronic pain patients and observational results have shown it to be effective in reducing anxiety, brain fog, and depression in patients with PT...
What is the current status of trial NCT04421573?
This trial is currently recruiting. It is a NA study. The enrollment target is 24 participants. The study started on 2023-07-10. Estimated completion is 2027-10-01.
What conditions does trial NCT04421573 study?
This clinical trial studies the following conditions: PTSD. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04421573?
The interventions under investigation include: BCPHD with D5W (PROCEDURE), Waiting period with usual care (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04421573?
This trial is sponsored by Dr. Dean Reeves Clinic, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04421573 being conducted?
This trial has 4 study locations across Kentucky, Oregon, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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