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Investigating the effectiveness of eicosapentaenoic acid on Inflammatory biomarkers and Quality of life on ischemic stroke patients

Investigating the effectiveness of eicosapentaenoic acid on Inflammatory biomarkers and Quality of life on ischemic stroke patients: a randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260201068719N1
Enrollment
135
Registered
2026-02-18
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

ischemic stroke. Cerebral infarction

Interventions

Intervention 1: First intervention group: Nutrition enriched with eicosapentaenoic acid with a dose of 2 grams daily. Intervention 2: Second intervention group: Nutrition enriched with eicosapentaenoi

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with ischemic stroke who are hospitalized Patients with Age over 18 years

Exclusion criteria

Exclusion criteria: Patients who are treating with Alteplase Patients with history of allergy and intolerance to cod liver oil and its derivatives Patients with platelet levels less than 50,000 Patients with bleeding peptic ulcer Pregnant women Patients with severe stroke with a NIHSS score over 20

Design outcomes

Primary

MeasureTime frame
Inflammatory biomarkers include high-sensitivity C-reactive protein (hs-CRP), tumor necrosis factor alpha (TNF-a), and interleukin-6 (IL-6). Timepoint: Inflammatory biomarkers including include high-sensitivity C-reactive protein, tumor necrosis factor alpha, and interleukin-6 will be measured at the beginning of the study and one month and three months after the start of the study. Method of measurement: Inflammatory biomarkers, including hs-CRP (by Latex-Enhanced Immunoturbidimetry) will be measured on a biochemical autoanalyzer (Hitachi model). Serum levels of interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-a) will also be measured using commercial ELISA kits with a sandwich method according to the manufacturer's instructions and optical absorption reading in an ELISA Reader at the appropriate wavelength (usually 450 nm) on fasting serum samples. All measurements will be performed in the central study laboratory in compliance with quality control protocols.;Neurologic Deficits. Timepoint: Neurologic Deficits will be measured at the beginning of the study and one month and three months after the start of the study. Method of measurement: The National Institutes of Health Stroke Scale (NIHSS) will be used to quantitatively assess neurological deficits. This 15-item scale assesses the patient's condition in various domains, including level of consciousness, motor function, vision, language, and attention. The assessment will be performed by a trained neurologist at specific study time points (baseline, one month, and three months after intervention). The total NIHSS score will be calculated and recorded for each patient.;Quality of Life. Timepoint: Quality of Life will be measured at the beginning of the study and one month and three months after the start of the study. Method of measurement: To assess the quality of life of patients, the Persian version of the Stroke-Specific Quality of Life Scale (SS-QOL) will be used. This 49-item questionnaire measure

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamaneh Masoudi

Shahid Beheshti University of Medical Sciences

drsmasoudi@yahoo.com+98 21 7343 2574

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026