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The effect of vitamin C supplementation on oxidative stress indices and skin repigmentation of patient with vitiligo

The effect of vitamin C supplementation on oxidative stress indices and skin repigmentation of patient with vitiligo

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230123057193N1
Enrollment
44
Registered
2023-04-17
Start date
2023-04-08
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Vitiligo. L80- Diseases of the skin and subcutaneous tissue.

Interventions

Intervention 1: Intervention group will receive daily 1 tablets of vitamin C 1000 mg with water for 8 weeks. Vitamin C tablets will be purchased from the Gol-darou Company with C Fix brand. All the pa

Sponsors

Research assistant of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Definitive diagnosis of vitiligo by a dermatologist, without gender restrictions Newly diagnosed vitiligo patient (under one month) or less than 10 phototherapy sessions Adults 20-60 years old

Exclusion criteria

Exclusion criteria: Being pregnant or breastfeeding Underlying diseases, including malignancy, history of kidney stones, other chronic and inflammatory diseases except vitiligo Taking antibiotics, antivirals and antifungals Use of vitamin C supplements and antioxidants in the last 3 months Any history of alcohol and tobacco use

Design outcomes

Primary

MeasureTime frame
Catalase. Timepoint: Baseline and 8 weeks after intervention. Method of measurement: ELISA assay.

Secondary

MeasureTime frame
Regimentation. Timepoint: Baseline and 8 weeks after intervention. Method of measurement: vitiligo area scoring index (VASI) score.;Superoxide dismutase. Timepoint: ?????? ?????? (??? ?? ???? ??????) ? 8 ???? ?? ?? ??????. Method of measurement: ELISA assay.;Total oxidant status. Timepoint: Baseline and 8 weeks after intervention. Method of measurement: ELISA assay.;Total antioxidant capacity. Timepoint: Baseline and 8 weeks after intervention. Method of measurement: ELISA assay.;Malondialdehyde. Timepoint: Baseline and 8 weeks after intervention. Method of measurement: ELISA assay.;Glutathione peroxidase. Timepoint: Baseline and 8 weeks after intervention. Method of measurement: ELISA assay.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoraiya Ebrahimpour-koujan

Tehran University of Medical Sciences

nutri.seam1@gmail.com+98 21 5563 0553

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026