Intensive Versus Standard Treatment for Spinal Anesthesia-induced Hypotension on Maternal Hemodynamics

Launched by GENERAL HOSPITAL OF NINGXIA MEDICAL UNIVERSITY · Nov 28, 2023

Keywords

ClinConnect Summary

This clinical trial is studying how different blood pressure targets during a cesarean section affect mothers' health after the surgery. Specifically, it looks at whether maintaining higher or standard blood pressure levels helps improve how mothers feel and recover after spinal anesthesia, which is often used during cesarean deliveries.

Women between the ages of 18 and 45 who are pregnant with a single baby and scheduled for a cesarean section may be eligible to participate. To join, participants should be in good health and not have certain medical conditions, like high blood pressure or low hemoglobin levels. If you decide to participate, you can expect close monitoring during and after the procedure to see how your body responds to the different blood pressure strategies. This trial aims to ensure mothers have better outcomes after surgery, and your involvement could help improve care for others in the future.

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• • 18-45 years
• • Primipara or multipara
• • Singleton pregnancy ≥37 weeks
• • American Society of Anesthesiologists physical status classification I to II
• • Scheduled for cesarean section under spinal anesthesia
• Exclusion Criteria:
• • Body height \< 150 cm
• • Body weight \> 100 kg or body mass index (BMI) ≥ 40 kg/m2
• • Eclampsia or chronic hypertension or baseline blood pressure ≥180 mmHg
• • Hemoglobin \< 7g/dl
• • Fetal distress, or known fetal developmental anomaly