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Recruiting Observational

Effect of Vitamin D Deficiency on the Frequency and Severity of Spinal Anesthesia-Induced Hypotension in Pregnant Women Undergoing Cesarean Section

NCT07057362 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-03-01
Last updated
2026-01-06

Condition(s) studied

Spinal Anesthesia-induced HypotensionVitamin D DeficiencyCesarean Section

Investigational drug(s) / intervention(s)

Intraoperative Hemodynamic Monitoring

Intraoperative Hemodynamic Monitoring: Continuous intraoperative monitoring of systolic blood pressure and heart rate following spinal anesthesia. Vasopressor usage and total fluid administration will be recorded.

Study summary

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

Sex
FEMALE
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Pregnant women aged 18 years or older * Scheduled for elective cesarean delivery under spinal anesthesia * Able and willing to provide written informed consent Exclusion Criteria: * 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 * Inability to undergo blood sampling or provide valid hemodynamic data * Contraindication to spinal anesthesia

Primary outcome measure(s)

  • Incidence of Hypotension After Spinal Anesthesia — ntraoperative (0-30 minutes after spinal anesthesia)
    Hypotension is defined as a ≥20% decrease in systolic blood pressure from baseline or an absolute systolic value \<90 mmHg. The presence or absence of hypotension will be recorded.

Trial sites (1)

FacilityCityRegionStatus
Duzce University Faculty of Medicine, Department of Anesthesiology and Reanimation Düzce Merkez Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07057362 on ClinicalTrials.gov ↗ ← All trials in Turkey