Clinical Trial

Predicting Spinal Hypotension in Cesarean Section

Study acronym: prediction
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Summary
This prospective observational study investigates the predictive value of anthropometric and hemodynamic indices for spinal anesthesia-induced hypotension (SAIH) during cesarean section. While spinal anesthesia is preferred for its rapid onset, SAIH remains a frequent complication risking maternal and fetal safety. The study enrolled parturients at Erciyes University, excluding those with hypertension or extreme weight/height. Preoperative measurements included BMI, waist circumference (WC), body roundness index (BRI), and modified shock index (MSI). Following standardized spinal anesthesia with hyperbaric bupivacaine (Harten's dosage), hemodynamic parameters and sensory block levels were monitored. This research aims to determine whether BRI and WC offer superior predictive utility compared with conventional markers such as BMI and MSI to enhance individualized risk assessment in obstetric anesthesia.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-03-25.
Trial Details
NCT Number NCT07499947
Lead Sponsor TC Erciyes University
Conditions Spinal Anesthesia, Cesarean Section, Hypotension
Enrollment 321 participants
Start Date 2026-03-16
Primary Completion 2026-10-20 (estimated)
Study Completion 2026-11-30 (estimated)
Updated on ClinicalTrials.gov 2026-03-31