NCT05685628 Evaluation of the Quality of Life Induced by the Cinnamon Anti-odor Dressing in Patients With Malodorous Wounds
| NCT ID | NCT05685628 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Condition | Malodorous Wounds (Chronic, Malignant or Infected Wounds) |
| Study Type | INTERVENTIONAL |
| Enrollment | 98 participants |
| Start Date | 2023-10-04 |
| Primary Completion | 2027-04-19 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 98 participants in total. It began in 2023-10-04 with a primary completion date of 2027-04-19.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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 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.
Contact & Investigator
Isabelle FROMANTIN, IDE
STUDY DIRECTOR
Institut Curie
Frequently Asked Questions
Who can join the NCT05685628 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Malodorous Wounds (Chronic, Malignant or Infected Wounds). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05685628 currently recruiting?
Yes, NCT05685628 is actively recruiting participants. Contact the research team at maxime.cheron@curie.fr for enrollment information.
Where is the NCT05685628 trial being conducted?
This trial is being conducted at Vaux-le-Pénil, France, Créteil, France, Créteil, France, Levallois-Perret, France and 3 additional locations.
Who is sponsoring the NCT05685628 clinical trial?
NCT05685628 is sponsored by Assistance Publique - Hôpitaux de Paris. The principal investigator is Isabelle FROMANTIN, IDE at Institut Curie. The trial plans to enroll 98 participants.