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Investigating the effect of vitamin D on discoid lupus erythematosus

The effectiveness of vitamin D injection compared to placebo on disease severity in patients with discoid lupus erythematosus

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220506054753N1
Enrollment
30
Registered
2024-01-31
Start date
2022-09-23
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

Discoid lupus erythematosus. Discoid lupus erythematosus

Interventions

Intervention 1: Intervention group: taking oral vitamin D3 1000 tablets once a day for 3 months produced by Abidi factory. Intervention 2: Control group: taking placebo once a day for 3 months.

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Aged over 18 years Patients with DLE whose initial diagnosis based on clinical manifestations was confirmed during a histopathological study of a skin sample sent to the pathology department Referred to the dermatology clinic of Sina Hospital in Tabriz Providing Informed consent

Exclusion criteria

Exclusion criteria: Systemic lupus erythematosus Active kidney disease Hepatitis Malabsorption syndrome Corticosteroid, dietary supplements and contraceptives, or anticonvulsants (phenytoin and phenobarbital) users People with liver enzymes over 40 Abnormal sensitivity to vitamin D Pregnant women

Design outcomes

Primary

MeasureTime frame
The severity of discoid lupus erythematosus using CLAS criteria. Timepoint: Measurements before starting treatment and after 3 months of oral vitamin D treatment. Method of measurement: Cutaneous LE Disease Area and Severity Index (CLAS) criteria.

Secondary

MeasureTime frame
Vitamin D levels. Timepoint: Before and after the treatment period 3 months. Method of measurement: Individuals will undergo venous blood draw from the Antecubital area after 14-14 hours of fasting. The obtained samples will be measured by vitamin D level by quantitative luminescence method.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahareh Mehramuz

Tabriz University of Medical Sciences

mehramuzb@tbzmed.ac.ir+98 41 3337 3901

Outcome results

None listed

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