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Aclarion Announces Addition of University of Arizona College of Medicine – Phoenix as CLARITY Trial Site

Aclarion (Nasdaq: ACON) announced that the University of Arizona College of Medicine – Phoenix has been added as a new clinical site in its CLARITY trial, bringing the total to ten actively enrolling centers.

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Aclarion (Nasdaq: ACON) announced that the University of Arizona College of Medicine – Phoenix has been added as a new clinical site in its CLARITY trial, bringing the total to ten actively enrolling centers. CLARITY is a prospective, randomized, multi-center study evaluating the company’s Nociscan SaaS platform in patients undergoing fusion or total disc replacement surgery for discogenic low back pain.

The 300-patient trial’s primary endpoint is change in back pain on a 100mm VAS Back scale at 12 months versus baseline, with several secondary endpoints. Aclarion anticipates an initial internal data readout and an expected public disclosure of early interim CLARITY results in Q4 2026. According to Aclarion, Nociscan uses MR Spectroscopy and augmented intelligence to quantify chemical biomarkers associated with disc pain, and has demonstrated a 97% surgical success rate when all Nociscan‑positive discs are treated.

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Argus Aug 20 session 1 alert
-3.61% close to close 1.1x rel. volume Open Argus
Details

Market move: ACON -3.61% in the Aug 20 session. CLARITY trial site addition

$7.61M Market Cap

On Aug 20, the day this news came out, ACON closed 3.61% below the previous close.

Data tracked by StockTitan Argus for the Aug 20 session.

Key Figures

Active enrolling sites: 10 sites Study size: 300 patients Primary endpoint scale: 100mm VAS Back +4 more
Active enrolling sites
10 sites
CLARITY study
Study size
300 patients
CLARITY prospective randomized study
Primary endpoint scale
100mm VAS Back
Back pain measurement
Endpoint assessment
12 months
Compared with baseline
Interim results timing
Q4 2026
Expected public disclosure of early interim results
Affected population
Approximately 266 million people
Worldwide degenerative spine disease and low back pain
Surgical success rate
97%
When all Nociscan-positive discs are treated

Historical Context

5 past events · Latest: Aug 12
5 events
  1. Aug 12

    Patent allowance

    24h Move
    +0.9%

    USPTO notice advanced patent protection for Nociscan's MRS scan process.

  2. Aug 04

    Provider site expansion

    24h Move
    +0.8%

    Nociscan became available at Indiana's first offering site.

  3. Jul 29

    Shareholder progress update

    24h Move
    -5.4%

    Letter reported scan growth, reimbursement progress, cash, and CLARITY developments.

  4. Jul 21

    Clinical abstracts

    24h Move
    -3.4%

    Two ASPN abstracts highlighted real-world Nociscan use and reported outcomes.

  5. Jul 07

    Trial site addition

    24h Move
    -2.6%

    Texas Spine Care Center joined the 300-patient CLARITY trial.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Key Terms

mr spectroscopy, discogenic low back pain, prospective, randomized clinical trial
3 terms
mr spectroscopy medical
"Nociscan’s ability to improve surgical outcomes for chronic low back pain Nociscan® aims"
MR spectroscopy is a scientific technique that uses magnetic fields and radio waves to analyze the chemical composition of materials, including biological tissues. It helps researchers identify and measure the presence of different molecules, providing insights into health, disease, or material properties. For investors, understanding MR spectroscopy can be important when evaluating innovations in medical technology or pharmaceutical developments that may impact healthcare markets.
discogenic low back pain medical
"patients undergoing surgical treatment (Fusion / TDR) for discogenic low back pain"
Pain that comes from one or more spinal discs, the cushion-like pads between the bones of the lower spine, usually because of wear, tear, injury or internal disc damage; these discs can bulge, crack, or lose height and irritate nearby nerves or tissues. It matters to investors because its prevalence drives demand for diagnostics, pain treatments, medical devices and surgical procedures, affecting healthcare spending, company revenue and regulatory attention in related markets.
prospective, randomized clinical trial technical
"Ten sites now actively enrolling in CLARITY study, a prospective, randomized clinical trial"
A prospective, randomized clinical trial is a study in which participants are enrolled and followed forward in time while being randomly assigned to different treatments or to a control group. Random assignment works like a lottery or coin flip to reduce bias so differences in outcomes are more likely due to the treatments themselves. Investors watch these trials because their results carry weight with regulators, affect approval and adoption chances, and can materially change a therapy’s commercial prospects.

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  • University of Arizona College of Medicine – Phoenix is home to a leading neurosurgery and orthopedic spine program with deep expertise in complex spine surgery and a strong commitment to clinical research and innovation
  • Ten sites now actively enrolling in CLARITY study, a prospective, randomized clinical trial designed to demonstrate Nociscan’s ability to improve surgical outcomes for chronic low back pain
  • Nociscan® aims to become the gold standard in identifying sources of low back pain through MR Spectroscopy (MRS) and Augmented Intelligence (AI)

BROOMFIELD, Colo., Aug. 20, 2026 (GLOBE NEWSWIRE) -- Aclarion, Inc., (“Aclarion” or the “Company”) (Nasdaq: ACON, ACONW), a healthcare technology company that is leveraging biomarkers and proprietary augmented intelligence (AI) algorithms to help physicians identify the location of chronic low back pain, today announced the University of Arizona College of Medicine - Phoenix as a new clinical site in its CLARITY (Chronic Low bAck pain Randomized Independent Trial studY) trial. The groundbreaking CLARITY study is designed to demonstrate Nociscan's clinical and economic value in spine surgery.

The University of Arizona College of Medicine – Phoenix is home to a nationally recognized neurosurgery and orthopedic spine program with expertise in complex and minimally invasive spine surgery, advanced neuromodulation, and translational research. The program's integration of clinical care, research and education makes it a natural fit for the CLARITY trial network.

“Chronic low back pain remains one of the most challenging problems in spine surgery, not because we lack the ability to treat it, but because identifying the precise disc responsible for a patient's pain has historically been imprecise. When I agreed to serve as Principal Investigator for the CLARITY trial, it was because I believed Nociscan represented a meaningful advance in our ability to objectively measure the chemical biomarkers associated with disc pain,” said Nicholas Theodore, MD, FACS, FAANS, Chairman of Neurosurgery, University of Arizona College of Medicine – Phoenix at Banner – University Medical Center Phoenix, and Principal Investigator, CLARITY trial. “Having the University of Arizona College of Medicine – Phoenix participate as a trial site allows my team to contribute directly to generating the evidence needed to establish Nociscan as a standard of care for surgical decision making in chronic low back pain.”

The University of Arizona College of Medicine - Phoenix joins a growing network of high-volume CLARITY trial sites including Johns Hopkins University, Northwestern Medicine, Advocate Aurora Research Institute, Texas Back Institute, Keck Medicine at USC, UHealth — University of Miami Health System, Scripps Health, Lanman Spinal Neurosurgery, and Texas Spine Care Center.

The CLARITY trial is a 300-patient, prospective, randomized, multi-center study evaluating Nociscan in patients undergoing surgical treatment (Fusion / TDR) for discogenic low back pain. The primary endpoint is change in back pain as measured on a 100mm VAS Back at 12 months compared to baseline, with several secondary endpoints collected. The company anticipates having an initial internal data readout and an expected public disclosure of early interim results in Q4 2026.

"Having Dr. Theodore's institution as an active CLARITY trial site adds another dimension to his leadership as Principal Investigator," said Ryan Bond, Chief Strategy Officer of Aclarion. "The University of Arizona College of Medicine – Phoenix brings exceptional clinical and research capabilities to the trial, and we are proud to have Dr. Theodore and his team contributing directly to the evidence we are building for Nociscan."

Chronic low back pain is a global healthcare problem with approximately 266 million people worldwide suffering from degenerative spine disease and low back pain. Aclarion’s Nociscan solution is the first evidence-supported SaaS platform to noninvasively help physicians distinguish between painful and nonpainful discs in the lumbar spine. Nociscan objectively quantifies chemical biomarkers demonstrated to be associated with disc pain. When used with other diagnostic tools, Nociscan provides critical insights into the location of a patient’s low back pain and demonstrates a 97% surgical success rate when all Nociscan-positive discs are treated.

For more information about CLARITY, please visit: CLARITY Trial

To find a Nociscan center, view our site map here.

For more information on Nociscan, please email: info@aclarion.com

All organizations cited and/or quotes from individuals not part of Aclarion have reviewed and approved the contents herein.

About Aclarion, Inc.

Aclarion is a healthcare technology company that leverages Magnetic Resonance Spectroscopy (“MRS”), proprietary signal processing techniques, biomarkers, and augmented intelligence algorithms to optimize clinical treatments. The Company is first addressing the chronic low back pain market with Nociscan, the first, evidence-supported, SaaS platform to noninvasively help physicians distinguish between painful and nonpainful discs in the lumbar spine. Through a cloud connection, Nociscan receives magnetic resonance spectroscopy (MRS) data from an MRI machine for each lumbar disc being evaluated. In the cloud, proprietary signal processing techniques extract and quantify chemical biomarkers demonstrated to be associated with disc pain. Biomarker data is entered into proprietary algorithms to indicate if a disc may be a source of pain. When used with other diagnostic tools, Nociscan provides critical insights into the location of a patient’s low back pain, giving physicians clarity to optimize treatment strategies.  For more information, please visit www.aclarion.com.

Forward Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 about the Company’s current expectations about future results, performance, prospects and opportunities. Statements that are not historical facts, such as “anticipates,” “believes” and “expects” or similar expressions, are forward-looking statements. These forward-looking statements are based on the current plans and expectations of management and are subject to a number of uncertainties and risks that could significantly affect the Company’s current plans and expectations, as well as future results of operations and financial condition.  Forward-looking statements in this release include, among others, statements regarding the enrollment of patients in our ongoing clinical trial, the growing interest in integrating Nociscan into real-world clinical workflows, having an initial internal data readout and the expected public disclosure of early interim results in Q4 2026 and, the continued expansion of the CLARITY trial to generate the high-quality evidence needed to advance Nociscan. These and other risks and uncertainties are discussed more fully in our filings with the Securities and Exchange Commission. Readers are encouraged to review the section titled “Risk Factors” in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025, as well as other disclosures contained in the Prospectus and subsequent filings made with the Securities and Exchange Commission. Forward-looking statements contained in this announcement are made as of this date and the Company undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

Investor Contacts:

Kirin M. Smith
PCG Advisory, Inc.
ksmith@pcgadvisory.com

Media Contacts:

Jennie Kim
SPRIG Consulting
jennie@sprigconsulting.com


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What did Aclarion (NASDAQ: ACON) announce about the CLARITY trial on August 20, 2026?

Aclarion announced that the University of Arizona College of Medicine – Phoenix joined its CLARITY trial as a new clinical site, bringing the network to ten enrolling centers. According to Aclarion, this institution adds advanced neurosurgery and spine research capabilities to the Nociscan-focused chronic low back pain study.

What is the design of Aclarion’s CLARITY trial evaluating Nociscan (ACON)?

CLARITY is a 300-patient, prospective, randomized, multi-center clinical trial studying Nociscan in patients receiving fusion or total disc replacement for discogenic low back pain. According to Aclarion, the primary endpoint is change in back pain on a 100mm VAS Back scale at 12 months versus baseline.

When does Aclarion expect interim CLARITY trial results for Nociscan (ACON)?

Aclarion expects an initial internal data readout and public disclosure of early interim CLARITY results in Q4 2026. According to Aclarion, these interim data will relate to Nociscan’s clinical and economic value in guiding surgical treatment for discogenic chronic low back pain.

How does Aclarion’s Nociscan technology help identify sources of chronic low back pain?

Nociscan uses MR Spectroscopy and augmented intelligence algorithms to quantify chemical biomarkers associated with disc pain. According to Aclarion, this evidence-supported SaaS platform helps physicians noninvasively distinguish between painful and nonpainful lumbar discs and provides critical insights when combined with other diagnostic tools for surgical decision making.

What surgical success rate is associated with Nociscan according to Aclarion (ACON)?

According to Aclarion, Nociscan demonstrates a 97% surgical success rate when all Nociscan-positive discs are treated. This reported rate reflects outcomes when Nociscan’s biomarker-based findings guide which lumbar discs receive surgical intervention in patients with discogenic chronic low back pain.

How many sites are currently enrolling in Aclarion’s CLARITY trial and which major centers are involved?

Ten sites are actively enrolling in CLARITY, including University of Arizona College of Medicine – Phoenix, Johns Hopkins University, Northwestern Medicine, Advocate Aurora Research Institute, Texas Back Institute, Keck Medicine at USC, UHealth – University of Miami Health System, Scripps Health, Lanman Spinal Neurosurgery, and Texas Spine Care Center.

What medical need is Aclarion targeting with the CLARITY trial and Nociscan?

CLARITY targets discogenic chronic low back pain, a condition within degenerative spine disease affecting about 266 million people globally. According to Aclarion, Nociscan aims to improve identification of painful discs, supporting better surgical decision making and potentially improving outcomes in fusion and disc replacement procedures.

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