Atopic Dermatitis
Conditions
Keywords
atopic dermatitis, aristocort, triamcinolone acetonide
Brief summary
This study is a randomized, intraindividual study to evaluate the short-term efficacy of triamcinolone acetonide (Aristocort® C) in subjects with atopic dermatitis.
Detailed description
This study is being conducted to evaluate the short-term efficacy and effect of triamcinolone acetonide (Aristocort® C) on pruritus, skin biomarkers and skin parameters in subject with atopic dermatitis. Approximately 20 subjects with atopic dermatitis will receive twice-daily topical application of triamcinolone acetonide (Aristocort® C) or vehicle in two different randomized areas for 3 days.
Interventions
On Day 1, Day 2, and Day 3, subjects will receive 2 applications of 3 mg/cm2 on the same lesional area, at an interval of approximately 12 ± 2 hours.
DRUGVehicle
On Day 1, Day 2, and Day 3, subjects will receive 2 applications of 3 mg/cm2 on the same lesional area, at an interval of approximately 12 ± 2 hours.
Sponsors
Innovaderm Research Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Intervention model description
Intra-individual
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Male or female subjects 18 years of age or older at the time of consent. 2. Subject has clinically confirmed diagnosis of active AD, according to Hanifin and Rajka criteria. 3. Subject has at least a 6-month history of AD and had no significant flares in AD for at least 4 weeks before screening. 4. Subject has 2 applications areas (10 X 10 cm) with a lesional surface of at least 6 X 6 cm, preferably located on 2 distinct anatomical areas at Day 1.
Exclusion criteria
1. Subject is a female who is breastfeeding, pregnant, or who is planning to become pregnant during the study. 2. Subject has clinically infected AD. 3. Subject has a Fitzpatrick's Skin Phototype ≥5. 4. Subject has a history of skin disease or presence of skin condition, other than AD, that would interfere with the study assessments in the opinion of the investigator. 5. Subject is known to have immune deficiency or is immunocompromised. 6. Subject has a history of cancer or lymphoproliferative disease within 5 years prior to Day 1. 7. Subject has any clinically significant medical condition that would, in the opinion of the investigator, put the subject at undue risk or interfere with interpretation of study results. 8. Subject has a known history of chronic infectious disease. 9. Subject has a known or suspected allergy to triamcinolone acetonide (Aristocort® C) or any component of the investigational product.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in pruritus NRS on AD lesions | 72 hours | The intensity of pruritus will be evaluated using a NRS by asking subjects to assign a numerical score to the worst level of itching at each application area in the past 12 hours, on a scale from 0 to 10, where 0 indicates no itch and 10 indicates the worst imaginable itch. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in pruritus NRS on AD lesions | 12, 24, 36, 48, and 60 hours | The intensity of pruritus will be evaluated using a NRS (Numeric Rating Scale) by asking subjects to assign a numerical score to the worst level of itching at each application area in the past 12 hours, on a scale from 0 to 10, where 0 indicates no itch and 10 indicates the worst imaginable itch. |
| Change from baseline in skin biomarkers for AD | Day 2, Day 3, and Day 4 | An untargeted biomarker approach with gene expression profile of treated and untreated skin samples will be performed. |
| Change from baseline in TSS | Day 4 | The TSS (Total Sign Score) is an assessment of the severity of erythema, edema/papulation, oozing/crusting, excoriation, lichenification, and dryness, each scored independently using the 4-point severity scale with a value range from 0 to 3 (clear to severe). The rating for each parameter is then summed to create a score ranging from 0 to 18. |
| Change from baseline in TAA | Day 4 | The TAA (Target Areas Assessment) is a 6-point scale with a value range from 0 to 5 (clear to very severe) used to evaluate AD severity at each site of study drugs application. |
| Change from baseline in lesion IGA | Day 4 | The lesion IGA (Investigator Global Assessment) is a 5-point scale with a value range from 0 to 4 (clear to severe) used for the assessment of each target lesion severity. |
Countries
Canada
Outcome results
None listed