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Evaluation of the effect of two drugs, memantine and celecoxib, on the number of seizures in patients with treatment-resistant seizures and changes in serum levels of inflammatory factors.

Evaluation and comparison of the effectiveness of two drugs, memantine and celecoxib, on seizure frequency in treatment-resistant epileptic patients, as well as changes in serum levels of the inflammatory factor interleukin-1 following medication interventions

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250923067340N1
Enrollment
75
Registered
2025-10-02
Start date
2025-10-26
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

Treatment-resistant seizures. Epilepsy, unspecified

Interventions

Intervention 1: Intervention group: Eligible treatment-resistant epileptic patients are supposed to receive memantine. In fact, in this group, patients are prescribed memantine at a dose of 10 mg at n

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Treatment-resistant epileptic patients

Exclusion criteria

Exclusion criteria: Patients with brain anatomical problems such as temporal sclerosis and cerebral encephalitis Patient with a history of intracranial hemorrhage, stroke, acute ischemic attack, concussion, and cerebral vascular thrombosis Chronic kidney disease Chronic liver disease such as Cirrhosis and ascites Pregnancy and lactation History of cardiovascular disease such as myocardial infarction, angina pectoris, scleroderma, systemic vascular hypertension, and pulmonary arterial hypertension History of gastrointestinal bleeding and inflammatory bowel disease Active gastrointestinal ulcer Concomitant use of medications that increase the risk of bleeding, such as anticoagulants and antiplatelets Ages over 55 years old and under 18 years old

Design outcomes

Primary

MeasureTime frame
Seizure frequency. Timepoint: baseline and month 6. Method of measurement: Clinical outcome assessment in seizure frequency changes according to a questionnaire developed by a neurologist.;Serum interleukin 1 level. Timepoint: baseline and month 6. Method of measurement: Patients are evaluated at time intervals of zero (baseline) and month 6 to check the level of the inflammatory factor interleukin-1 in taken blood samples.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Mohammadgholizad

Ardabil University of Medical Sciences

pha.fa.chess@gmail.com+98 45 3352 2437

Outcome results

None listed

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