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The effect of supplementation with alpha lipoic acid on serum levels of factors, disease enzymes, lipid fractions and oxidative stress in patients with psoriasis

The effect of supplementation with alpha lipoic acid on serum levels of factors, disease enzymes, lipid fractions and oxidative stress in patients with psoriasis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230123057193N3
Enrollment
44
Registered
2024-03-29
Start date
2024-04-13
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Psoriasis. Diseases of the skin and subcutaneous tissue

Interventions

Intervention 1: Intervention group: The intervention group will receive 1 tablet of alphalipoic acid at a dose of 600 mg with water for 8 weeks. Alphalipoic acid tablets are purchased from Karen B. Al

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Diagnosis of psoriasis based on the PASI criteria by a dermatologist PASI number above 20 in psoriasis patients

Exclusion criteria

Exclusion criteria: Any history of alcohol and tobacco use Breastfeeding and pregnancy or pregnancy intention within the next 3 months Use of biological drugs, corticosteroids, methotrexate, antibiotics Having diabetes and the presence of any diagnosed neoplasia or malignancy Use of antioxidants and omega-3 supplements in the last 3 months

Design outcomes

Primary

MeasureTime frame
ESR. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the intervention. Method of measurement: Elisa.;ALT, AST, ALKP. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the intervention. Method of measurement: Elisa.;TG, TC, HDL, LDL. Timepoint: At the beginning of the study (before the start of the intervention) and 8 weeks after the intervention. Method of measurement: Elisa.

Secondary

MeasureTime frame
CRP. Timepoint: The beginning of the intervention (before the intervention) and after 8 weeks of the intervention. Method of measurement: Elisa.;MDA. Timepoint: The beginning of the intervention (before the intervention) and after 8 weeks of the intervention. Method of measurement: Elisa.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactsorayia ebrahim pour 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 4, 2026