Can wound fluid reveal the best healing therapies?
NCT ID NCT07745764
First seen Aug 04, 2026 · Last updated Aug 05, 2026 · Updated 1 time
Summary
This study collects wound fluid and tissue samples from 72 adults with chronic, non-healing ulcers, such as diabetic foot ulcers or surgical wounds. Researchers will use these samples in laboratory tests to see how different wound healing treatments, including INJECTHEAL hydrogel components, affect cell growth and bacteria. The goal is to find biomarkers that predict which treatments might work best for individual patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- INJECTHEAL hydrogel components and other wound healing therapeutics tested in laboratory assays using patient wound samples
- What this could lead to
- If successful, this could help identify which wound healing treatments work best for chronic ulcers and guide the development of more effective therapies.
- What could go wrong
- This is an observational study using lab tests, not a clinical treatment trial. Results may not directly translate to real-world healing outcomes, and the sample size is small.
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 72 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2028
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
Adults with chronic, non-healing deep cavity wounds, such as diabetic foot ulcers, arterial ulcers of the lower extremity, post-surgical non-healing wounds, or wounds with delayed healing, who are treated as part of routine clinical care and who undergo routine negative pressure wound therapy and/or medically indicated sharp or surgical debridement.
- 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: * Age ≥ 18 years * Type I or type II diabetes with lower extremity deep cavity ulcers * Arterial leg ulcers with lower extremity deep cavity ulcers * Surgical deep cavity non-healing wounds * Wounds with delayed healing * Routine treatment with negative pressure wound therapy * Routine sharp or surgical debridement * Sufficient wound exudate available (min. of 2 ml per visit) * Patient is informed about the study and has given informed consent Exclusion Criteria: * Age ≤ 18 years * Multiple substance abuse (poly-toxicomania) * No signed declaration of consent or incapable of giving an informed written consent * Proven active infections with HIV, hepatitis C or HPV * Active pregnancy
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Heinrich-Heine University, Duesseldorf
Düsseldorf, 40225, Germany