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Vitamin D treatment in allergic skin rashes

Therapeutic Effect of Single Dose Vitamin D3 in Childhood Atopic Dermatitis ? A Prospective Clinical Trial.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/07/014727
Enrollment
73
Registered
2018-07-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: L209- Atopic dermatitis, unspecified Health Condition 2: L209- Atopic dermatitis, unspecified

Interventions

Intervention1: Vitamin D3: Single dose Vitamin D3 will be given to children with atopic dermatitis Control Intervention1: Not applicable: Not applicable

Sponsors

Intramural funds Institute Ethics Committee
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All Children with atopic dermatitis from the age group of 1 year till 14 years attending JIPMER Pediatrics and Dermatology OPD will be recruited and single oral dose Vitamin D3 ( 1,20,000 IU) will be given at enrolment.

Exclusion criteria

Exclusion criteria: 1) Children with chronic underlying disease on immunosuppressive therapy (Neurological/cardiac/metabolic/respiratory/gastrointestinal) 2) Children with known or suspected immunodeficiency. 3) Children on prolonged antibiotic therapy and Anti tuberculous therapy. 4) Children who are a part of other studies.

Design outcomes

Primary

MeasureTime frame
EVALUATION OF CLINICAL SEVERITY OF ATOPIC DERMATITIS AND DECREASE IN SCORAD LEVELS OVER A P FALL IN IgE ANTIBODY TITRES FALL IN ABSOLUTE EOSINOPHIL COUNTSTimepoint: OUTCOMES WILL BE ASSESSED AT THE END OF 4 MONTHS, AFTER GIVING SINGLE DOSE VITAMIN D

Secondary

MeasureTime frame
1) To assess the change in serum 25(OH) D levels after single oral dose ( 1,20,000 IU ) Vitamin D3 supplementation. 2) To assess the change in absolute eosinophil counts and IgE antibody titres after Vitamin D supplementation. 3) To assess the reduction in the number of exacerbations. Timepoint: 4 months

Countries

India

Contacts

Public ContactDhayalini RK

Jawaharlal Institute Of Postgraduate Medical Education and Research

drnbiswal@yahoo.com9442528402

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026