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New suction device for surgical wounds enters first human safety trial

NCT ID NCT06259409

Recruiting now Symptom relief Sponsor: Progenerative Medical, Inc Source: ClinicalTrials.gov ↗

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This early-stage trial is testing whether a new device called Regenn® Negative Pressure Therapy System is safe for people recovering from spinal fusion surgery. The device applies gentle suction to the surgical wound to help manage healing. About 30 adults will be randomly assigned to receive either the new device or a similar existing device. Researchers will track serious complications, pain levels, and other side effects over three months.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance
Regenn® Negative Pressure Therapy System (a device that applies gentle suction to a surgical wound)
What this could lead to
If safe, this device could offer a new option for managing surgical wounds after spinal surgery, potentially reducing complications.
What could go wrong
This is a very early (Phase 1) safety study with only 30 people. It is not designed to prove the device works better than existing options, and unexpected side effects are possible.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

injury lumbar disk degenerative disorder spondylolisthesis Surgical Wound

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

SURGICAL WOUND

Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

  • Contact

    Email: •••••@•••••

Locations

  • The University of Kansas Medical Center

    RECRUITING

    Kansas City, Kansas, 66160, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.