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

Recruiting now · Not applicable

Conditions studied: Malodorous Wounds (Chronic, Malignant or Infected Wounds)

In brief

Refer to "Detailed description".

Key facts

Study ID

NCT05685628

Run by

Assistance Publique - Hôpitaux de Paris

People needed

98

Starts

2023-10-04

Expected to finish

2027-04-19

Last updated by the study team

2026-05-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• Patient who has received a secondary charcoal or cinnamon dressing within the last 48 hours
• 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.

Where it is running

• Hospitalisation à Domicile AP-HP — Paris, France (enrolling)
• Institut Curie — Paris, France (enrolling)
• Hôpital Henri Mondor — Créteil, France (enrolling)
• Hôpital Sainte Périne — Paris, France
• Hospitalisation à domicile Fondation Santé Service — Levallois-Perret, France
• Hôpital Henri Mondor — Créteil, France
• Hospitalisation à domicile de la région de Melun — Vaux-le-Pénil, France, France

Full record on ClinicalTrials.gov

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