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Effect of sodium selenium administration on functional and cognitive scores in ischemic stroke

Investigation of the sodium selenium administration on the level of inflammatory factors, oxidative stress and functional and cognitive scores in acute ischemic stroke patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170104031773N3
Enrollment
60
Registered
2019-06-09
Start date
2019-04-21
Completion date
Unknown
Last updated
2019-08-26

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: 500µg Selenase injection vial contains 1.67mg sodium selenite pentahydrate (German biosyn company), receiving a dose of 2000 µg after admission and then 1000 µg for 5 days. Interventio

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with acute stroke

Exclusion criteria

Exclusion criteria: Receiving antioxidants constantly (such as vitamin C and E) Receiving anti-inflammatory drugs constantly(steroids, nonsteroidal anti-inflammatory) Suffered from HIV and neurodegenerative diseases (e.g. Alzheimer's, Parkinson's, amyotrophic lateral sclerosis, multiple sclerosis) Systemic diseases such as Diabetes Mellitus, Renal Failure, Malignant Melanoma, Uremia,Myopathy, and Congestive Heart Failure Loss of consciousness level due to any reason except stroke (such as shock, alcohol consumption or intoxication)

Design outcomes

Primary

MeasureTime frame
The level of tumor necrosis factor alpha(TNF-a). Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking sodium selenite. Method of measurement: Blood sample.;The level of superoxide dismutase (SOD). Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking sodium selenite. Method of measurement: Blood Sample.;The level of glutathione peroxidase(GPx). Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking sodium selenite. Method of measurement: Blood Sample.

Secondary

MeasureTime frame
Motor function and verbal. Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking sodium selenite. Method of measurement: National Institues of Health Stroke Scale Questionnaire.;Cognitive performance. Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking sodium selenite. Method of measurement: Mini Mental State Examination Questionnaire.;Degree of disability. Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking sodium selenite. Method of measurement: Modified Rankin Scale Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Simani

Shahid Beheshti University of Medical Sciences

l.simani90@sbmu.ac.ir+98 21 5102 5182

Outcome results

None listed

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