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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-40
SponsorDuzce University

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

Treatment groups

140 Participants
are divided into 2 treatment groups

Sponsors and collaborators