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New treatment option for Malodorous Wounds (Chronic, Malignant or Infected Wounds)
Official title Evaluation of the Quality of Life Induced by the Cinnamon Anti-odor Dressing in Patients With Malodorous Wounds
ClinicalTrials.gov ID: NCT05685628
What this study is testing
- What it's testing
- Refer to "Detailed description".
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join 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 likely can't join 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;
See the full eligibility 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
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Vaux-le-Pénil, France, France
- Créteil, France
- Levallois-Perret, France
- Paris, France
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Vaux-le-Pénil, France, France; Créteil, France; Levallois-Perret, France; Paris, France. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.