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Evaluation of Topical B12 for the Treatment of Childhood Atopic Dermatitis

Evaluation of Topical B12 for the Treatment of Childhood Atopic Dermatitis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00465699
Enrollment
50
Registered
2007-04-25
Start date
2007-04-30
Completion date
2007-04-30
Last updated
2007-04-25

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

Conditions

Eczema

Keywords

Eczema, Pediatric, Vitamin B12

Brief summary

This study is being done to see in B12 applied to the skin will improve the symptoms of eczema in children compared to a placebo creme

Detailed description

INTRODUCTION: Atopic dermatitis is a prevalent disease process in children, affecting up to 20% of children in the United States. Various treatment options are available to treat atopic dermatitis to include topical emollients, topical steroids, and topical calcineurin inhibitors. Each treatment option has benefits and potential risks. This study was done to determine if topical B12 could be a tolerable and efficacious alternative treatment option in this population. METHODS: The study was conducted as a placebo-controlled, double-blind, prospective, randomized clinical trial with intraindividual left ⁄ right comparison. Parents were given 2 containers of creams and instructed to apply the Vitamin B12 cream to one side of the body and the placebo cream to the contralateral side according to the randomization scheme.

Interventions

DRUGTopical B12 0.07%

Sponsors

Spartanburg Regional Healthcare System
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
6 Months to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* children presenting to the Center for Family Medicine or Regional Pediatrics between the ages of 6 months and 18 years old with atopic dermatitis

Exclusion criteria

* unwillingness of parent to consent to study protocol, pregnancy or lactation, eczema with superinfection present, known history of allergy to Vitamin B12 or components of the base cream, topical treatment with corticosteroids in the 4 weeks prior to enrollment

Design outcomes

Primary

MeasureTime frame
Reduction in SCORAD at 2 and 4 weeks

Countries

United States

Contacts

Primary ContactRonald P Januchowski, D.O.
rjanuchowski@srhs.com864-560-1558
Backup ContactMary E Johnson
mejohnson@srhs.com864-560-6892

Outcome results

None listed

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