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Effect of vitamin D in enhanced recovery after brain surgery

Phase 3
Recruiting
Conditions
Patients with brain tumors who have candidate for craniotomy surgery.
Malignant neoplasm of brain
Registration Number
IRCT20190126042496N1
Lead Sponsor
eurofunctional Reseach Center of Shohada Tajrish Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

The willingness to cooperate and complete the informed consent form by the patient or legal surrogate
The patient's age = 18
Definitive diagnosis of brain tumor and need craniotomy for resection
Levels of 25-OHD = 20 ng/mL for intervention group
Levels of 25-OHD > 30 ng/mL for normal group

Exclusion Criteria

Unwillingness to co-operate by the patients or their surrogate at the beginning of the study
Participation in other clinical trials at the same time with this study
Pregnancy and lactation
Hypercalcemia
Hyperphosphatemia
Tuberculosis
Sarcoidosis
History of nephrolithiasis

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes in serum levels of 25OHD before and after injection and surgery. Timepoint: Measurement of serum levels of 25OHD at the beginning of the study in all patients. Measurement of serum levels of 25OHD on the fifth day after surgery in intervention group who received a single high dose of vitamin D prior to surgery. Method of measurement: Laboratory measurements of 25OHD serum levels using Monobind kit by Enzyme-Linked Immunosorbent Assay (ELISA) method.
Secondary Outcome Measures
NameTimeMethod
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