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ACTIVE NOT RECRUITING NA

Multicenter Single-arm Trial to Investigate Clinical Outcomes When Cohealyx™ is Used for Full Thickness Wounds

NCT06787690 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this study is to look at clinical outcomes when Cohealyx Collagen Matrix is used to treat full thickness wounds after surgical excision in patients that require a skin graft to heal their wounds. The main question it aims to answer is how long does it take for Cohealyx to support definitive closure.

Interventions

  • DEVICE Cohealyx

Study Locations (18)

Arizona

  • Valleywise Health — Phoenix
  • University of Arizona — Tucson

Ohio

  • Akron Children's Hospital — Akron
  • Ohio State University — Columbus

Texas

  • JPS Health Network — Fort Worth
  • Texas Tech University — Lubbock

Alabama

  • University of South Alabama — Mobile

District of Columbia

  • Medstar Washington Hospital Center — Washington D.C.

Iowa

  • Univ of Iowa — Iowa City

Kansas

  • The University of Kansas Health — Kansas City

Kentucky

  • University of Louisville — Louisville

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2025-05-15
Est. Completion 2026-08
Phase NA

Sponsor

Avita Medical

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06787690

The ClinicalTrials.gov registry entry for NCT06787690 describes a study currently listed as active not 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 41 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Avita Medical, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Surgical Wound appearing as the primary indexed condition, and to 1 intervention — of which Cohealyx 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: NCT06787690 reports 18 study locations spanning 15 distinct geographic areas — top geographies include Arizona, Ohio, Texas. 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 NCT06787690 about?

NCT06787690 is a clinical study titled "Multicenter Single-arm Trial to Investigate Clinical Outcomes When Cohealyx™ is Used for Full Thickness Wounds". The goal of this study is to look at clinical outcomes when Cohealyx Collagen Matrix is used to treat full thickness wounds after surgical excision in patients that require a skin graft to heal their wounds. The main question it aims to answer is how long does it take for Cohealyx to support definit...

What is the current status of trial NCT06787690?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 41 participants. The study started on 2025-05-15. Estimated completion is 2026-08.

What conditions does trial NCT06787690 study?

This clinical trial studies the following conditions: Surgical Wound, Burn, Trauma Wound, Full Thickness Wounds. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06787690?

The interventions under investigation include: Cohealyx (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06787690?

This trial is sponsored by Avita Medical, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06787690 being conducted?

This trial has 18 study locations across Alabama, Arizona, District of Columbia, Iowa, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial