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NCT06263140 Clinical Trial

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

Vitamin D Deficiency Clinical Trial

Official title:
A Study of Vitamin D Levels in Patients With Non-immediate Drug Hypersensitivity, Case-control Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06263140
Other study ID # Chula-ARC 001/21
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 30, 2021
Est. completion date February 1, 2022

Study information
Verified date February 2022
Source Chulalongkorn University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date February 1, 2022
Est. primary completion date January 15, 2022
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Thailand Faculty of Medicine, Chulalongkorn University Bangkok

Sponsors (1)
Lead Sponsor Collaborator
Chulalongkorn University

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary Serum vitamin D levels Serum vitamin D levels at baseline At baseline
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