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Amniotic membrane grafts show promise for stubborn wounds

NCT ID NCT07223281

Disease control Sponsor: Legacy Medical Consultants Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether adding amniotic membrane products to standard wound care helps diabetic foot ulcers, venous leg ulcers, and pressure ulcers heal faster. Researchers will compare healing rates in 2,400 adults treated with these grafts versus those receiving standard care alone. The main goal is to see if more wounds close completely within 12 weeks with the added treatment.

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

Study facts

What this study's own registry entry says, in plain language.

Participants

About 2,400 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2025

Expected to finish

Dec 2025

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Patients with DFU, VLU, or PU

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults ≥18; DFU/VLU/PU; sufficient observable timeline Exclusion Criteria: * Use of other advanced wound products, atypical ulcer etiology (e.g., malignancy, vasculitis); insufficient follow-up

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Conditions

The condition(s) this trial relates to.

decubitus ulcer Diabetic Foot ulcer of lower limbs

As listed by the trial registrant

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

Diabetic foot ulcer (DFU) Pressure ulcers, bedsores, decubitus ulcer Venous leg ulcers (VLUS)

Contacts and locations

Locations

  • Advanced Wound Therapy

    Tulsa, Oklahoma, 74137, United States

  • Colorado Foot and Ankle

    Colorado Springs, Colorado, 80903, United States

  • Comprehensive Occupational Medicine

    Nitro, West Virginia, 25143, United States

  • Podiatric Surgical Specialists

    Clinton Township, Michigan, 48038, United States

More trials for these conditions

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