Predicting Spinal Hypotension in Cesarean Section

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorTC Erciyes University

About this trial

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.

Eligibility criteria

Qualifiers

American Society of Anesthesiologists (ASA) Class II

Having regular antenatal visits

Singleton pregnancy at ≥37 weeks of gestation

Pregnant women aged 18-45 -

Disqualifiers

Those with eclampsia, those with preeclampsia

Undergoing an emergency cesarean section

Those with bleeding diathesis and those receiving anticoagulant therapy

With a history of carotid artery stenosis,

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

321 Participants
are grouped into 1 trial group

Sponsors and collaborators