Clinical Trial

Preoperative Data and the Spinal Spread of Local Anesthetic in Cesarean Section

Completed
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Summary
This study is designed to assess possible relation between the anthropometric data of pregnant women at term, as well as their babies, and the maximal level of sensory blockade following spinal anesthesia for cesarean section. The debate regarding this relation is ongoing. Although there is some relevant data in favor of both lack and the presence of significant relation between these variables, it is still not clear whether the same dose of local anesthetic is similarly effective, regardless of parturient's and fetal size.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-09-21.
Status change: Recruiting → Completed 2026-05-28
Trial Details
NCT Number NCT07197398
Lead Sponsor Centre of Postgraduate Medical Education
Conditions Spinal Anesthesia Evaluation, Cesarean Delivery
Enrollment 183 participants
Start Date 2025-09-18
Primary Completion 2025-11-30 (estimated)
Study Completion 2025-12-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-01