Umbilical cord particles show promise for stubborn wounds
NCT ID NCT07414368
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This small study is testing Corplex P, a device made from donated human umbilical cord tissue, to see if it helps heal wounds that won't close on their own, like diabetic foot ulcers. Ten people will receive the device as part of their standard wound care. Researchers will track how many wounds fully close within 12 weeks and how quickly they heal.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Corplex P (dehydrated human umbilical cord particulate)
- What this could lead to
- If it works, this could point toward a simple, natural way to help stubborn wounds heal faster and more completely.
- What could go wrong
- This is a very small, early study with only 10 people and no comparison group. Results may not apply to everyone, and the device might not work better than standard care alone.
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
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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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
Consecutive subjects receiving Corplex P in a real-world setting
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * All consecutive subjects that received a Corplex P device application during wound management in the following retrospective cohort between February 2024 and November 2025. Exclusion Criteria: * Subjects not receiving an initial Corplex P application during treatment
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Family Foot & Ankle Specialists, LLC
Bridgeport, Connecticut, 06606, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Cameras and ultrasound could take the guesswork out of wound care
- Zapping a leg nerve: can a wearable device help stubborn ulcers heal?
- Wound dressings that trap microbes: scientists test a Drug-Free approach
- Can a muffin help heal stomach ulcers?
- Can a placental patch help heal stubborn diabetic foot ulcers?
- Can a united team heal stubborn ulcers faster?