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Recruiting NCT05685628

Evaluation of the Quality of Life Induced by the Cinnamon Anti-odor Dressing in Patients With Malodorous Wounds

Trial Parameters

Condition Malodorous Wounds (Chronic, Malignant or Infected Wounds)
Sponsor Assistance Publique - Hôpitaux de Paris
Study Type INTERVENTIONAL
Phase N/A
Enrollment 98
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2023-10-04
Completion 2027-04-19
Interventions
Cinnamon dressingCharcoal dressing

Brief Summary

Refer to "Detailed description".

Eligibility Criteria

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.

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