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The Therapeutic Effects of Topical Cannabidiol (CBD) Products for Atopic Dermatitis

Recruiting
Conditions
Atopic Dermatitis
Interventions
Other: Phoilex Releaf Gel
Registration Number
NCT06022874
Lead Sponsor
Phoilex Ltd.
Brief Summary

The goal of this observational study is to learn about the potential therapeutic effects of topical CBD products produced by Phoilex Ltd., specifically the Releaf Gel, in those diagnosed with atopic dermatitis. Patients will be routinely assessed via questionnaire, and physical measurements will be taken with respect to the affected area studied in order to judge clinical efficacy.

The main question\[s\] it aims to answer are:

* Did you experience an immediate increase in skin hydration?

* Did you experience a soothing or comforting feeling on your irritated skin area? Please explain where your affected area is located, and also include at what time point this occurred. Example: Affected Area: Palm, Time Point: 1-hour post-application

* Upon the affected area being in the healing phase, was your skin itch/scratch free for 4/6/10/12 hours (please circle)?

* Did you experience immediate relief from your skin inflammation?

* Did the study cream absorb quickly into your skin, without any greasy feeling?

* Has your skin flare disappeared in 2 week(s)?

* Has your skin condition appearance improved? (Yes/No)

Participants will apply Phoilex Releaf Gel (a cream) to their affected areas of atopic dermatitis. The questions listed above shall be discussed and observations recorded at the 0 week, 1 week, 2 week, and 4 week time points. Additional monitoring questions may be asked of the participants to ensure the safety of the product. A chart will be provided to the participants to track Phoilex Releaf Gel usage (how many pumps, and time of day) throughout duration of the study.

We hypothesize that Releaf gel will be suitable to ameliorate the common signs and symptoms of atopic dermatitis as well as improve patient quality of life.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Specifically, patients would be recruited based on the following inclusion criteria must be over 18 years old and must be diagnosed with moderate-to-severe eczema.
Exclusion Criteria
  • Exclusion criteria would include not currently using any steroids or biologics, not currently using any other topical products, not pregnant, not breast feeding, nor have any allergies to any ingredients listed within the formula of the Releaf gel. A negative pregnancy test will need to be confirmed prior to patient receiving Phoilex Releaf Gel. Lastly, participants who have been diagnosed with anxiety or depression with a classification of greater than mild anxiety or mild depression will be excluded. As such, screening for possible candidates for the clinical trial will include questions and a brief assessment on participants mental health by study doctor/physician.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Patient's Diagnosed with Atopic DermatitisPhoilex Releaf GelPatient's Diagnosed with Atopic Dermatitis
Primary Outcome Measures
NameTimeMethod
Will topically applied CBD be effective in reducing the appearance/clearing of atopic dermatitis after 4 weeks of study treatment?5 weeks

Outcome will be measured based on observations recorded at 0 weeks, 1 week, 2 week, and 4 week time point, not limited to physical assessment, clinical photography, and the responses of questions below:

* Did you experience an immediate increase in skin hydration?

* Did you experience a soothing or comforting feeling on your irritated skin area? Please explain where your affected area is located, and also include at what time point this occurred. Example: Affected Area: Palm, Time Point: 1-hour post-application

* Upon the affected area being in the healing phase, was your skin itch/scratch free for 4/6/10/12 hours (please circle)?

* Did you experience immediate relief from your skin inflammation?

* Did the study cream absorb quickly into your skin, without any greasy feeling?

* Has your skin flare disappeared in 2 week(s)?

* Has your skin condition appearance improved? (Yes/No)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Phoenix Medical Spa X Peak Human

🇨🇦

Brampton, Ontario, Canada

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