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A comparison of the efficacy and safety of 0.1% adapalene gel and 0.025% tretinoin cream in the treatment of childhood acanthosis nigricans

Phase 4
Completed
Conditions
childhood acanthosis nigricans
Acanthosis nigricans
childhood
Topical retinoid
Registration Number
TCTR20170603001
Lead Sponsor
Faculty of Medicine, Srinakhariwirot University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
20
Inclusion Criteria

The participants aged 12 -18 years with a diagnosis of acanthosis nigricans

Exclusion Criteria

- Vulnerable skin diseases
- Infectious skin diseases
- Other recent diseases involving the neck
- Other serious medical disorders e.g. DM, liver disease
- Any patients having received other therapies for up to 4 weeks prior to enrollment.
- Photosensitive skin
- Immunocompromised host
- Pregnancy and lactation
- Receiving oral retinoids
- Neck tattoo

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
erythema index and melanin index at the baseline, at week 2, 4 and 8. Mexameter
Secondary Outcome Measures
NameTimeMethod
The efficacy of the treatment at the baseline, at week 2, 4 and 8. investigator’s global evaluation (IGE) scale and the parent’s global evaluation (PGE)
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