RecruitingNot ApplicableNCT05685628

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

Evaluation of the Quality of Life Induced by the Cinnamon Anti-odor Dressing in Patients With Malodorous Wounds: a Multicenter Randomized Controlled Trial


Sponsor

Assistance Publique - Hôpitaux de Paris

Enrollment

98 participants

Start Date

Oct 4, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Refer to "Detailed description".


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Charcoal dressing and Cinnamon dressing for people with malodorous wounds (chronic, malignant or infected wounds). The study is currently recruiting participants at 7 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERCinnamon dressing

Use of CINESTEAM® as a non-occlusive secondary dressing CE marked medical device class I, secondary, absorbent, non-adhesive and composed of: * Anti-odor upper part, adsorbent containing cinnamon powder. * Weakly absorbent lower part intended to absorb excess exudates.

OTHERCharcoal dressing

Use of a secondary non-occlusive activated charcoal dressing (brand of your choice)


Locations(7)

Hospitalisation à domicile de la région de Melun

Vaux-le-Pénil, France, France

Hôpital Henri Mondor

Créteil, France

Hôpital Henri Mondor

Créteil, France

Hospitalisation à domicile Fondation Santé Service

Levallois-Perret, France

Hospitalisation à Domicile AP-HP

Paris, France

Institut Curie

Paris, France

Hôpital Sainte Périne

Paris, France

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NCT05685628