Neurowell Clinical Research

Our PTSD Research

We're evaluating whether an investigational combination of two long-approved treatments can help restore healthy brain energy signaling in PTSD. This IRB oversight study provides active treatment, no placebo, clinical monitoring, and personalized dose optimization.

IRB Oversight

Institutional review board approved protocol

Active Treatment – No Placebo

Every participant receives active treatment

Specialist Care Team

Led by board-certified physicians

Why This Study

Targeting Brain Energy,Not Just Symptoms

Emerging research suggests PTSD involves disrupted astrocyte-neuron energy support and dysregulated cellular "energy switches." HB-01 is designed to address these pathways by combining two established medicines to support energy production and coordination. Use in PTSD is investigational and is being evaluated in this trial.

Energy support hypothesis

Improve mitochondrial output and fuel routing to key circuits.

Network coordination hypothesis

Normalize astrocyte signaling to reduce 'energy crisis' states.

Whole-person monitoring

Cognitive, functional, and safety assessments at each visit.

How It Works

HB-01 (Two Components, Dual Target)

A

PPAR-γ Pathway Support

A long-approved treatment hypothesized to help shift astrocytes from "conserve" to "support" mode and bolster mitochondrial efficiency. Safety monitored throughout.

B

Calcium Signaling Balance

A well-established medicine hypothesized to stabilize astrocyte activity and reduce inefficient over-excitation in stress networks.

Rationale: Pairing production + distribution support may yield broader effects than either alone.

Who May Qualify

Eligibility Snapshot

Likely Candidates

Adults (18+) with diagnosed PTSD or trauma-related symptoms
Persistent brain fog, mental fatigue, or emotional blunting
Limited response to prior treatments
Stable on current treatment (4+ weeks)
Willing to complete study visits and assessments

Key Exclusions

Active substance use disorder
Pregnant or planning pregnancy during the study
Severe uncontrolled cardiovascular conditions
Other criteria per screening by the study physician
Study Benefits
Active treatment for all (no placebo) participants
Treatment and study visits provided at no cost
Specialist oversight with regular safety monitoring
Advanced Assessments
Metabolic and cognitive measures to track changes
Personalized dose optimization
Optional plain-friendly summaries for your records

Fast Next Step

A confidential phone screen determines fit and answers your questions.

How Symptoms Can Arise

Metabolic Mismatch

Under stress, astrocytes may prioritize conservation over support, reducing efficient fuel delivery to circuits that govern cognition and emotion.

Cellular "Switches"

Energy Sensing

AMPK/mTOR signaling helps cells balance survival vs. performance; dysregulation is an active research focus in stress-related disorders.

Network Effects

Calcium Coordination

Astrocyte calcium activity coordinates local networks; instability can impair synchrony and resilience under stress.

"It felt like someone turned the lights back on. I could think clearly and be present again."

, Study participant, Week 8 (individual experience; results vary)

What To Expect

Three Simple Steps

01

Screen

Confidential call to review history and eligibility.

02

Evaluate

Baseline visit, labs as indicated, and assessments.

03

Begin

Start HB-01 with regular check-ins and optimization.

Contact

Take the First Step

Our research team will answer questions and discuss eligibility.

Frequently Asked Questions

Important Information & Disclaimers: HB-01 combines two FDA-approved treatments for other conditions. Its safety and efficacy for PTSD are investigational and are being evaluated in this IRB oversight clinical study. The information above is not medical advice. You will receive and should review the informed consent documents before deciding whether to participate.