Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07375160

Evaluation of the Safety and Efficacy of Dehydrated Human Placenta Tissue (dHPT) for Wound Healing

The retrospective trial is observational, intended to stand alone, complement and integrate data collected in ongoing clinical studies to aid in establishing payor coverage in the United States (U.S.) for Cellution Biologics allograft products with real-world evidence to support the clinical adoption in patients to manage chronic or surgical wounds.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

About this study

Around 10.5 million Medicare beneficiaries were affected by chronic wounds in 2019. A chronic wound is generally defined as any wound that fails to heal within a reasonable timeframe. Chronic wounds can be categorized into the following four groups: arterial, pressure, diabetic, and venous. Despite the well-established standard of care for chronic wounds, which includes sharp debridement, offloading, and maintaining proper moisture balance, a notable gap remains between historical outcomes and desired results in chronic wound care.

One approach to treating chronic wounds involves the use of dehydrated human placental tissues, which are defined as 'A broad category of biomaterials, synthetic materials, or biosynthetic matrices that support repair or regeneration of injured tissues through various mechanisms of action. The application of dHTPs in chronic wound treatment provides several benefits, including creating a protective environment for healing, covering deep structures, aiding surgical closure, enhancing functional outcomes, and improving appearance. The cellular category of dHTPs includes allografts, which are human donor tissue samples intended for use in another human patient. Utilizing human amniotic membrane as an allograft displays considerable promise for chronic wound treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years of age or older.
  • Wound treated with Cellution Biologics AmchoPlast, a dehydrated human placental tissue (dHPT).
  • Wound present for greater than or equal to 30 days prior to treatment with dHPT.
  • Wound is not infected.
  • Wound surface area is greater than 1cm2 at initial assessment.
  • Clinical documentation of wound treatment.

Exclusion criteria

  • AmchoPlast dHPT product was not applied to wound.
  • HbA1C >12%.
  • Presence of active osteomyelitis.
  • Concurrent treatment for malignant disease.
  • Use of other advanced biologics during treatment period.

Treatment and study plan

dHPT, AIC

Biological

Sterile dehydrated Human Amnion - Intermediate Layer - Chorion Membrane Allograft

Primary outcomes

  1. Time to Closure for Target Ulcer

    Time frame: Up to 8 months.

    To evaluate the time to wound closure for patients treated with dHPT.

Study contacts

Contact information is provided by the study sponsor or research team.

Bryanna Finstein

CONTACT

[email protected]

6035574660

Cellution Research

CONTACT

[email protected]

6035574660

Sponsors and collaborators

Lead sponsor

Cellution Biologics

Industry

Registry information

Official study title

A Retrospective, Real World Evidence (RWE) Trial to Evaluate the Safety and Efficacy of a Dehydrated Human Placenta Tissue (dHPT) for Wound Healing

Acronym: RETRO-PLAST

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 29, 2026
Registry last updated
Mar 3, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.