New tool aims to spot wound healing hurdles early
NCT ID NCT07334717
First seen Jun 27, 2026 · Last updated Aug 19, 2026 · Updated 2 times
Summary
This study is for people with wounds that have developed hypergranulation (overgrown tissue that slows healing). Researchers will take photos and use a new assessment tool to grade the severity. About 100 adults and children in the UK will take part. The goal is to create a standard way to measure hypergranulation, which will help design future treatments.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
-
3 people
The number who actually took part.
- Started
-
Apr 2026
- Finished
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Jun 2026
- 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
Approximately 80-100 participants who meet the inclusion criteria will be be recruited into the study. Participants will be recruited from tissue viability clinics, burns clinics and wound care clinics across the North West of England.
- Ages
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2 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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 * Male or female participants between 2 to 85 years of age (both inclusive). * Willing and able to provide written informed consent or assent (as applicable) as evidenced by signature on the participant's consent/assent form. In case if the child is providing assent, a caregiver or LAR must sign an informed consent. * A chronic HG wound which can be: * a VLU unhealed for a minimum of 6 weeks, but no longer than 24 weeks * an unhealed surgical wound that has been unhealed for at least 2 weeks but no longer than 24 weeks * a device entering the skin (eg, gastrostomy, suprapubic catheter, tracheostomy etc) that exhibits HG. * A degree of HG that is estimated to be raised at least 2 mm above the natural skin level, or above the base of the wound and an area of HG extending at least 10 mm in its longest length. * For VLU and surgical wounds, the wound should not have been healed by at least 25% area or length. * Have good general health as defined by: * medically fit enough to complete the study assessments * free of any other systemic condition that in the opinion of the Study Investigator may have an impact on the safety of the participant. * Be willing and able to attend all scheduled clinical assessments, (adults or caregiver) * able to communicate well with the Study Investigator and willing and able to comply with the expectations of the study. * This includes gastrostomy; suprapubic catheters, tracheostomy, other tube/catheter skin entry or exit sites, abdominal surgical wound, pilonidal sinus surgical site, split-skin donor site, plastic surgery sites, healing burn sites, peri-anal surgical wounds, gastrointestinal stoma, other. Exclusion Criteria * Unable to provide informed consent or assent * Unable to complete the scheduled study treatments and assessments * Have been previously recruited into this study * Participants who are \< 2 years or \>85 years of age
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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.
Contacts and locations
Locations
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EMS Healthcare
Ellesmere Port, Cheshire, CH65 4LE, United Kingdom
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Other studies related to the condition(s) this trial covers.
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