Please sign in to follow a disease.
Can nanotechnology silver beat standard gauze for diabetic foot ulcers?
NCT ID NCT07758855
First seen Aug 11, 2026 · Last updated Aug 12, 2026 · Updated 1 time
Summary
This trial compares a new silver-coated dressing made with nanotechnology to a standard saline-moistened gauze for treating infected diabetic foot ulcers. Adults with moderate (PEDIS grade 2 or 3) ulcers will receive either the silver dressing or conventional gauze, changed every 3 days for 21 days, alongside routine diabetic foot care. Researchers will measure changes in wound size, infection levels, and tissue health to see if the silver dressing improves healing and reduces infection better than standard care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A silver-coated wound dressing made with nanotechnology, applied directly to the ulcer and changed every 3 days for 21 days.
- What this could lead to
- If effective, this dressing could offer a better way to treat infected diabetic foot ulcers, potentially reducing the need for amputation and improving healing outcomes.
- What could go wrong
- This is a relatively small, early-stage study, and results may not apply to all patients. The dressing might not outperform standard care, and there is a risk of allergic reactions or skin irritation.
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
107 people
The number who actually took part.
- Started
-
May 2024
- Finished
-
Aug 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- 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 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: * Aged over 18 years * Able and willing to give written informed consent * PEDIS grade 2 or PEDIS grade 3 diabetic foot ulcer on either foot Exclusion Criteria: * Aged under 18 years * Known allergy to silver or to polyester * Pregnancy * Non-infected PEDIS grade 1 ulcer * PEDIS grade 4 ulcer, on the grounds of metabolic instability
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Diabetic ulcers on both feet are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
Ankara Bilkent City Hospital, Department of General Surgery
Ankara, Cankaya, 06800, Turkey (Türkiye)