Evaluation of the Quality of Life Induced by the Cinnamon Anti-odor Dressing in Patients With Mal… (NCT05685628) | Clinical Trial Compass
RecruitingNot Applicable
Evaluation of the Quality of Life Induced by the Cinnamon Anti-odor Dressing in Patients With Malodorous Wounds
France98 participantsStarted 2023-10-04
Plain-language summary
Refer to "Detailed description".
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patient \>18 years of age with a smelly wound (discomfort \> 4/10 expressed by the patient);
* Predictive wound healing \>14 days (clinical judgement);
* Patient benefiting from a social security scheme (AME excluded)
* Patient, and curator if applicable, informed and having signed the consent form for participation in the study
Exclusion Criteria:
* Patient already receiving a secondary charcoal or cinnamon dressing
* Patient with pressure ulcer stage 1 or 2
* Patient treated by metronidazole or antimicrobial for \< 3 days;
* Patient who cannot communicate his feelings;
* Anosmic patient;
* Patient with cinnamon allergy;
* Persons deprived of their liberty or under guardianship;
* Inability to submit to the medical follow-up of the trial for geographical, social, psychological or cognitive reasons.