About this trial
Spinal anesthesia-induced hypotension remains a common and significant complication during cesarean sections, posing risks for both mother and fetus. Vitamin D deficiency, frequently observed in pregnant women, is associated with altered vascular function and potential hemodynamic instability. This prospective observational study aims to investigate whether vitamin D deficiency is associated with an increased incidence and severity of spinal anesthesia-induced hypotension in pregnant women undergoing elective cesarean delivery. Vitamin D levels will be measured preoperatively, and intraoperative hemodynamic parameters will be closely monitored. The findings could contribute to improved management strategies for pregnant patients at risk of severe hypotension.
Eligibility criteria
Qualifiers
Pregnant women aged 18 years or older
Scheduled for elective cesarean delivery under spinal anesthesia
Able and willing to provide written informed consent
Disqualifiers
Emergency cesarean sections
History of significant cardiovascular disease (e.g., arrhythmia, heart failure)
Known neurological disorders affecting autonomic function
Current vitamin D supplementation within the past 30 days
Trial design
Treatments tested in this trial
- Intraoperative Hemodynamic Monitoring