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The effect of omega-3 on drug resistant epilepsy

The effect of omega-3 versus placebo on the clinical and paraclinical signs and symptoms of drug-resistant epileptic patients: a triple blind randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015062922142N2
Enrollment
40
Registered
2015-12-02
Start date
2015-12-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

epilepsy. Nonspecific epileptic seizures:•atonic

Interventions

Intervention 1: Standard treatment plus 300 mg (one tablet) omega-3 twice a day orally for 4 months. Intervention 2: Standard treatment plus a placebo tablet twice daily orally for 4 months.
Treatment - Drugs
Placebo
Standard treatment plus 300 mg (one tablet) omega-3 twice a day orally for 4 months
Standard treatment plus a placebo tablet twice daily orally for 4 months

Sponsors

hamadan university of medical sciences, Vice-chancellor for research and technology , Hamedan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: drug resistant epilepsy; 18 to 65 years old. Exclusion criteria: patients with impaired renal function; patients with catamenial seizure; Patients with hepatic dysfunction; Patients with active infection; Patients with brain or mental dysfunction; Patients who can not take oral medication; Patients treated with anti-inflammatory or antioxidant drugs in the past month; patients with other concurrent inflammatory disease; Patients who can not tolerate the side effects; Patients who are pregnant or lactating

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The frequency of attacks. Timepoint: Up to 4 months after the start treatment. Method of measurement: Quantitatively.

Secondary

MeasureTime frame
IL-6. Timepoint: Before the intervention-4 months after the treatment. Method of measurement: pg per ml by ELISA.;TNF-a. Timepoint: Before the intervention-4 months after the treatment. Method of measurement: pg per ml by ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Rasool Haddadi

Hamadan university of medical sciences, Faculty of pharmacy

haddadi.rasool@gmail.com; r.ghadermazi@gmail.com+98 81 3838 1593

Outcome results

None listed

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