Clinical Trial

Intra-abdominal Pressure, Abdominal Circumference, and Spinal Block Level in Cesarean Section

Completed
View on ClinicalTrials.gov →
Summary
Spinal anesthesia is commonly used for cesarean section and provides effective anesthesia with rapid onset. However, the spread of spinal anesthesia may vary among pregnant women due to physiological and anatomical changes during pregnancy. Increased intra-abdominal pressure and abdominal circumference may influence cerebrospinal fluid dynamics and affect the level of sensory block achieved after spinal anesthesia. This prospective observational study aims to evaluate the relationship between intra-abdominal pressure, abdominal circumference, and the maximum sensory block level following spinal anesthesia in pregnant women undergoing cesarean section. Intra-abdominal pressure and abdominal circumference will be measured before surgery, and sensory block levels and hemodynamic parameters will be assessed after spinal anesthesia. The findings of this study may help to better understand factors affecting spinal block spread in pregnant patients.
Protocol Amendment History 3 changes
critical Trial completed 2026-05-02
notable Primary completion pushed: 2026-02 -> 2026-04-01 2026-04-01
minor Completion pushed: 2026-03 -> 2026-04-15 2026-04-01
Trial Details
NCT Number NCT07406373
Lead Sponsor Kutahya Health Sciences University
Conditions Cesarean Section, Pregnancy, Elective Cesarean Section
Enrollment 107 participants
Start Date 2026-02-07
Primary Completion 2026-04-01 (estimated)
Study Completion 2026-04-30 (estimated)
Updated on ClinicalTrials.gov 2026-05-01