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Efficacy of Topical Pimecrolimus in the Treatment of Pityriasis Alba

Efficacy of Topical Pimecrolimus in the Treatment of Pityriasis Alba: A Randomized Placebo-controlled Trial

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03834935
Enrollment
40
Registered
2019-02-08
Start date
2019-03-01
Completion date
2021-04-01
Last updated
2019-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pityriasis Alba

Keywords

pityriasis alba, treatment, topical calcineurin inhibitor

Brief summary

Pityriasis alba (PA) is a common benign skin disorder, that usually affects children and adolescents of darker phototypes. A history of atopic dermatitis is a well-known risk factor, and PA may be a minor manifestation of atopic dermatitis, although it can occur in nonatopic individuals as well. The objective is to evaluate the effect of topical pimecrolimus in the treatment of treatment of PA

Detailed description

Background and Rationale: Pityriasis alba (PA) is a common benign skin disorder, that usually affects children and adolescents of darker phototypes. PA usually manifests as erythematous lesions followed by smooth scales with residual characteristic pruritic or non-pruritic ill-defined hypopigmented patches, that typically occur on the upper part of the body, especially the face. A history of atopic dermatitis is a well-known risk factor, and PA may be a minor manifestation of atopic dermatitis, although it can occur in nonatopic individuals as well. It is thought to represent nonspecific dermatitis with residual post-inflammatory hypopigmentation. Sun exposure is a triggering and accentuating factor. PA is a common reason for dermatologic consultation due to its chronic course, frequent relapses and cosmetic appearance. Spontaneous healing occurs in several months to few years, therefore impacting the quality of life. Emollients and mild-potency topical steroids are the mainstay of treatment, with a potential risk of skin atrophy and hypopigmentation. Pimecrolimus is a topical calcineurin inhibitor that prevents T-cell activation, approved for the treatment of atopic dermatitis, and proved efficacious for seborrheic dermatitis, without having the potential adverse effects of topical corticosteroids. Tacrolimus 0.1% ointment, another calcineurin inhibitor is an effective and safe treatment for PA, a similar efficacy of calcitriol and tacrolimus was shown after 9 weeks of treatment. An exploratory study evaluated the efficacy of pimecrolimus cream in the treatment of PA. To the best of our knowledge there is no randomized placebo-controlled trial in the literature proving the efficacy of pimecrolimus in PA. Objective: To evaluate the effect of topical pimecrolimus in the treatment of treatment of PA Hypothesis: Pimecrolimus is an efficacious, well-tolerated and safe treatment for pityriasis alba. Trial design: A randomized placebo-controlled double blinded trial establishing the superiority of topical pimecrolimus 1% over placebo.

Interventions

DRUGElidel (pimecrolimus 1%)

topical application of product on all lesions, twice daily. Sunscreen will not be indicated, and hygienic habits will not be changed

Topical application on all lesions, twice daily. Sunscreen will not be indicated, and hygienic habits will not be changed

Sponsors

St Joseph University, Beirut, Lebanon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

investigators and patients will be blinded to treatment

Eligibility

Sex/Gender
ALL
Age
2 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pityriasis alba Patients confirmed by a board certified dermatologist * Age over 2 years * Written informed consent signed by the patients or the legal guardians of patients younger than 18 years in the native language (Arabic)

Exclusion criteria

* Other concomitant dermatosis (except atopic dermatitis) * Use of topical steroids, or topical agents other than emollients and sunscreen, in the last 4 weeks * Known allergy to pimecrolimus * Pregnant and nursing women

Design outcomes

Primary

MeasureTime frameDescription
Percentage of repigmentation of index lesions9 weeksObjective percentage of repigmentation the index lesion (the largest lesion) by image analysis software (ImageJ software will be used to measure the lesion reduction area after treatments)

Secondary

MeasureTime frameDescription
Pruritus and scaling3,6 and 9 weeksIGA 4 point-scale (0: none - 3: severe)
Investigator's repigmentation change3,6 and 9 weeksClinical change is assessed by means of digital photographic registration (frontal, right, and left views). An independent observer clinically graded the global improvement as poor (0-25%), mild (26-50%), good (51-75%), and excellent (\>75%).
patient satisfaction9 weeks(0: not satisfied, 1: satisfied, 2: very satisfied).
Adverse events3,6 and 9 weeksadverse events reporting

Countries

Lebanon

Contacts

Primary Contactelio G kechichian, MD
elio.kechichian@gmail.com+9613079072

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026