New dressing may ease pain of incurable cancer wounds
NCT ID NCT07556146
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested two types of wound dressings in 31 cancer patients with inoperable malignant wounds. One dressing contained PHMB, a germ-fighting ingredient, and the other was a paraffin-based tulle. Researchers measured symptoms and quality of life over three months to see which dressing offered better relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- PHMB-containing dressing and paraffin-based tulle dressing
- What this could lead to
- If this works, it could point toward a better way to manage symptoms and improve quality of life for people with inoperable malignant wounds.
- What could go wrong
- This is a small, completed trial with only 31 participants, so results may not apply to everyone. It focuses on symptom relief, not healing the wound itself.
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
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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
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31 people
The number who actually took part.
- Started
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Dec 2023
- Finished
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Jun 2025
- Lead sponsor
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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
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * Patients aged 18 years and older * Diagnosed with cancer and having inoperable malignant wounds * Admitted to the wound care clinic * Able to provide informed consent Exclusion Criteria: * Patients with acute wounds * Patients with incomplete follow-up * Patients with conditions preventing adherence to the study protocol
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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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Sakarya Uni
Sakarya, Serdi̇van, 54000, Turkey (Türkiye)