Vitamin D Levels in Non-immediate Drug Hypersensitivity Case-control Study

Chulalongkorn University120 enrolled

Overview

Serum vitamin D levels in drug-induced non-immediate reactions

The study of serum vitamin D levels in patients presented with drug-induced non-immediate cutaneous adverse reactions compared to those in drug-tolerant control subjects

Study Type

OBSERVATIONAL

Enrollment

120

Conditions

Stevens-Johnson Syndrome Drug Reaction With Eosinophilia and Systemic Symptom Maculopapular Exanthem Vitamin D Deficiency Drug-Induced Rash

Eligibility

Sex: ALLMin age: 15 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Diagnosed with SJS/TEN, DRESS, AGEP, MPE, or FDE as mentioned above Exclusion Criteria: * Reactions from drugs with known strong genetic predispositions (allopurinol, carbamazepine, abacavir) * Receiving vitamin D supplement

Locations (1)

Faculty of Medicine, Chulalongkorn University

Bangkok, Thailand

Outcomes

Primary Outcomes

Serum vitamin D levels

Serum vitamin D levels at baseline

Time frame: At baseline

Data from ClinicalTrials.gov

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