Skip to content

Effect of high dose vitamin D on IL-ß blood level in patients with moderate stroke

Effect of high dose vitamin D on IL-1ß blood level in patients with moderate stroke: randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200213046484N2
Enrollment
42
Registered
2022-11-02
Start date
2022-11-21
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

cerebrovascular accident.

Interventions

Intervention 1: Intervention group: A single dose of vitamin D3, 300,000 units, IM. 1 ml vial .Manufacturing by DarouPakhsh factory. Intervention 2: Control group: Does not receive intervention (does

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with moderate stroke (NIHSS 5-15) Age between 18 to 65 years Vitamin D levels less than 30 ng/ml

Exclusion criteria

Exclusion criteria: Hypercalcemia (Ca > 10.5 mg/dl) Patients treated with corticosteroids, NSAIDs, statins History of diseases such as cancer, autoimmune disorders, liver diseases Pregnancy and breastfeeding History of allergy to vitamin D Poor chance of survival

Design outcomes

Primary

MeasureTime frame
IL1-ß. Timepoint: Before intervention and 3rd day after intervention. Method of measurement: Elisa kit.;Neutrophil to Lymphocyte Ratio (NLR). Timepoint: First to 7th day of the study on daily routine. Method of measurement: Calculating the ratio of Neutrophils to Lymphocytes using CBC test.;Platelet to Lymphocyte Ratio (PLR). Timepoint: First to 7th day of the study on daily routine. Method of measurement: Calculating the ratio of Platelet to Lymphocytes using CBC test.;National Institutes of Health Stroke Scale (NIHSS). Timepoint: First to 7th day of the study on daily routine. Method of measurement: Patient medical file.;Barthel Score. Timepoint: Three months after discharge. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Lenght of ICU stay. Timepoint: Daily. Method of measurement: Patient file.;Duraton of Mechanical Ventilation. Timepoint: Daily. Method of measurement: Patient file.;28-day mortality. Timepoint: 28th day of hospitalization. Method of measurement: Patient file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaied Amniati

Shahid Beheshti University of Medical Sciences

sa_amniati@yahoo.com+98 21 6651 5128

Outcome results

None listed

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