Actively Recruiting
Preoperative Data and the Spinal Spread of Local Anesthetic in Cesarean Section
Led by Centre of Postgraduate Medical Education · Updated on 2025-09-29
140
Participants Needed
1
Research Sites
10 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Preoperative Data and the Spinal Spread of Local Anesthetic in Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cesarean delivery at term under spinal anesthesia
- American Society of Anesthesiologists (ASA) physical status less than 3
- Body mass index (BMI) less than 40
You will not qualify if you...
- Spinal anesthesia with a dose other than 12.5 mg of hyperbaric bupivacaine
- Use of a local anesthetic other than hyperbaric bupivacaine
- Failed spinal anesthesia
- Poor quality or missing anesthetic records
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Centre of Postgraduate Medical Education,Department of Anesthesia and Intensive Care
Warsaw, Poland, 01-813
Actively Recruiting
Research Team
B
Bartosz Horosz, MD,PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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