NCT07057362 Effect of Vitamin D Deficiency on the Frequency and Severity of Spinal Anesthesia-Induced Hypotension in Pregnant Women Undergoing Cesarean Section
| NCT ID | NCT07057362 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Duzce University |
| Condition | Spinal Anesthesia-induced Hypotension |
| Study Type | OBSERVATIONAL |
| Enrollment | 140 participants |
| Start Date | 2025-03-01 |
| Primary Completion | 2025-12-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 140 participants in total. It began in 2025-03-01 with a primary completion date of 2025-12-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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 Criteria
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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07057362 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 40 Years, studying Spinal Anesthesia-induced Hypotension. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07057362 currently recruiting?
Yes, NCT07057362 is actively recruiting participants. Contact the research team at gizem123demir@hotmail.com for enrollment information.
Where is the NCT07057362 trial being conducted?
This trial is being conducted at Düzce, Turkey (Türkiye).
Who is sponsoring the NCT07057362 clinical trial?
NCT07057362 is sponsored by Duzce University. The trial plans to enroll 140 participants.