Evidence map›Paper›PMID 42244271›Full record

ArticleAnnals of dermatology2026

Crisaborole 2% for Pediatric Periorificial Dermatitis: A Randomized, Double-Blind, Vehicle-Controlled Pilot Study.

Ayelet Ollech, Bat-El Bar Aluma, Adi Weiss-Fink, Amir Horev, Ori Toker, Tali Czarnowicki

Abstract read
In one paragraph

Article in Annals of dermatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ayelet OllechPediatric Dermatology Service, Shaare Zedek Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel. ayeletol@szmc.org.il.ORCID https://orcid.org/0000-0003-0967-3968
Bat-El Bar AlumaPediatric Pulmonary Unit and Cystic Fibrosis Center, Lily and Edmond Safra Children's Hospital, Sheba Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID https://orcid.org/0000-0003-1944-427X
Adi Weiss-FinkClalit Health Services, Tel Aviv, Israel.ORCID https://orcid.org/0009-0006-9311-8017
Amir HorevPediatric Dermatology Service, and Ben Gurion University of the Negev Faculty of Health Sciences, Soroka University Medical Center, Beer Sheva, Israel.ORCID https://orcid.org/0000-0001-6646-9061
Ori TokerAllergy and Clinical Immunology Unit, Department of Pediatrics, Shaare Zedek Medical Center, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel.ORCID https://orcid.org/0000-0002-5248-3193
Tali CzarnowickiDr. Phillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.ORCID https://orcid.org/0000-0002-1157-5227

Funding

Pfizer company 57944115
6 · The paper itself

Abstract

backgroundPeriorificial dermatitis (POD) is a common inflammatory skin condition primarily affecting infants, children, and young women. Novel therapies such as phosphodiesterase 4 (PDE4) inhibitors provide promising non-steroidal anti-inflammatory treatment options.

objectiveThis study evaluated the efficacy and safety of topical crisaborole 2% ointment, a PDE4 inhibitor, for treating pediatric patients with POD.

methodsA randomized, double-blind, vehicle-controlled trial included 23 participants aged 3 months to 18 years. Patients were treated with crisaborole 2% ointment or placebo for 4 weeks, followed by a 4-week treatment-free observational period. Primary endpoints were a 50% reduction in the Perioral Dermatitis Severity Index (PODSI) and an Investigator's Global Assessment (IGA) score of 0 or 1 by day 14. Assessments were also conducted on days 29 and 58. Secondary measures included changes in Quality-of-Life Index scores over time and safety evaluations.

resultsBoth groups demonstrated improvement in PODSI and IGA scores during treatment. Although a small, non-significant numerical trend favored the crisaborole group across primary and secondary endpoints, no statistically significant differences between crisaborole and placebo were observed at any time point. Mild burning or stinging were reported more frequently in the crisaborole group, but they were generally tolerable.

conclusionWhile there was a modest numerical trend favoring crisaborole, its efficacy was not statistically superior to placebo in this small pilot study. Larger studies are needed to further validate the efficacy of crisaborole for the treatment for POD.

trial registrationClinical Trial Registry of the Ministry of Health of Israel Identifier: MOH_2020-05-12_008827.

Indexed as

Eczematous skin diseasesNon-steroidal anti-inflammatory agentPediatricsPerioral dermatitisPhosphodiesterase inhibitors

Identifiers

PMID42244271
PMCPMC13243719

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.