New study tests better bandages for bleeding cancer wounds
NCT ID NCT06581809
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether special hemostatic dressings can reduce bleeding when changing bandages on bleeding cancer wounds. Four adults with malignant wounds participated. Researchers compared bleeding and pain between hemostatic and regular dressings. The goal was to find a better way to manage bleeding and improve comfort during wound care.
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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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4 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Mar 2026
- 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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18 to 100 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients 18 years and older; * Carriers of a malignant wound ≥ 10cm²; * Possibility of participating simultaneously in another research study without an exclusion period at the end of the study; * Patient having signed an informed consent Exclusion Criteria: * Patient under 18 years of age; * Non-ulcerated nodule, tumor infiltration; * Patient in the terminal phase of their cancer; * Patients with a tumor wound that is a cutaneous melanoma; * Patient refusing to be managed by a private nurse or hospitalization at home (HAD); * Pregnant or breast-feeding women * Persons deprived of liberty or under guardianship (including curatorship); * Persons of legal age under court protection; * Inability to participate in the study for geographical, social, or psychological reasons.
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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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CHU Saint Eloi
Montpellier, 34090, France
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CLCC - Institut Godinot
Reims, 51100, France
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Centre François Baclesse
Caen, 14076, France
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EHPAD Claude Goudet
Marseillan, 34340, France
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EHPAD Laurent Antoine
Agde, 34300, France
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EHPAD Pergolines
Sète, 34207, France
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EHPAD l'Estagnol
Vias, 34450, France
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Groupe Hospitalier Diaconesses Croix Saint Simon
Paris, 75020, France
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Hôpital Saint Clair
Sète, 34200, France
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Hôpital Saint-Loup
Agde, 34300, France
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Hôpital Tenon
Paris, 75020, France
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Institut Curie
Paris, 75248, France