Skip to content

Effects of alpha-lipoic acid on patients undergoing hemodialysis

Evaluating the efficiency of alpha-lipoic acid supplementation on inflammatory biomarkers in hemodialysis patients: A double-blind placebo clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160206026390N12
Enrollment
92
Registered
2020-12-23
Start date
2017-08-23
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Patient undergoing hemodialysis. Chronic kidney disease, stage 5

Interventions

Intervention 1: The intervention group will receive alpha-lipoic acid supplements with a dose of 300 mg/day, The duration of the study will be for eight weeks. Intervention 2: The control group will c

Sponsors

Shahrekord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients (20-80 yr.) with a history of hemodialysis treatment for a minimum of six months Willing to participate in the trial

Exclusion criteria

Exclusion criteria: - Any recent significant changes in patients' lifestyle behaviors (diet, physical activity, stress) - History of consuming any antioxidant or anti-inflammatory dietary supplements less than one month before study enrollment - Possible kidney transplantation - History of alcohol consumption - History of cigarette smoking - Allergies or intolerance to alpha-lipoic acid - History of cancer

Design outcomes

Primary

MeasureTime frame
Total Antioxidant Capacity. Timepoint: Before and after study. Method of measurement: Laboratory kits.;Tumor necrosis factor- alpha. Timepoint: Before and after study. Method of measurement: Laboratory kits.;Erythroblast Sedimentation Rate. Timepoint: Before and after study. Method of measurement: Laboratory kits.;Interleukin - 6. Timepoint: Before and after study. Method of measurement: Laboratory kits.;C-reactive Protein. Timepoint: Before and after study. Method of measurement: Laboratory kits.;Irisin. Timepoint: Before and after study. Method of measurement: Laboratory kits.

Secondary

MeasureTime frame
Weight. Timepoint: Befor and after Study. Method of measurement: Sensitive Balance.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Javadian

Shahrekord University of Medical Sciences

javadianp@gmail.com+98 38 3222 0016

Outcome results

None listed

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