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Vitamin D in ischemic stroke

Investigating of vitamin D administration on the level of inflammatory factors and functional and cognitive scores in patients with cerebral ischemic stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170104031773N2
Enrollment
30
Registered
2019-03-08
Start date
2018-09-23
Completion date
Unknown
Last updated
2019-03-25

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: Injection of two vitamins D 3 with a dose of 300,000 units. The first dose is taken after confirmation vitamin D deficiency at the beginning of the disease, a

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 vitamin D deficiency (less than 20 ng per ml) Patients with moderate acute stroke based on the NIHSS scoring system

Exclusion criteria

Exclusion criteria: The serum level of vitamin D is above 20 ng per ml Receive antioxidants (such as vitamins C and E) continuously Receive continuous anti-inflammatory drugs (steroids-NSAIDs) AIDS and neurodegenerative diseases (such as Alzheimer's, Parkinson's, ALS, MS Systemic diseases like, Diabetes Mellitus, Kidney Failure, Malignant Melanoma, Uremia, Liver Cirrhosis and Chronic Myocardial Infarction, Myopathy Change in mental status with unknown etiology

Design outcomes

Primary

MeasureTime frame
The level of Tumor necrosis factor alpha. Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking vitamin D. Method of measurement: Blood sample.;The level of Interleukin 6. Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking vitamin D. Method of measurement: Blood sample.;The level of vitamin D. Timepoint: At the beginning of the study (before the intervention), 1 month after the start of taking vitamin D. Method of measurement: Blood Sample.

Secondary

MeasureTime frame
National Institues of Health Stroke Scale Measurement. Timepoint: At the beginning of the study (before the intervention), 1 and 3 months after the start of taking vitamin D. Method of measurement: National Institues of Health Stroke Scale Questionnaire.;Measuring Mini Mental State Examination. Timepoint: At the beginning of the study (before the intervention), 1 and 3 months after the start of taking vitamin D. Method of measurement: Mini Mental State Examination Questionnaire.;Measuring Modified Rankin Scale. Timepoint: At the beginning of the study (before the intervention), 1 and 3 months after the start of taking vitamin D. 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