Status:
RECRUITING
Preoperative Data and the Spinal Spread of Local Anesthetic in Cesarean Section
Lead Sponsor:
Centre of Postgraduate Medical Education
Conditions:
Spinal Anesthesia Evaluation
Cesarean Delivery
Eligibility:
FEMALE
18+ years
Brief 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 anesth...
Detailed Description
Spinal block is a gold standard of cesarean section anesthesia. Two major factors contribute to its popularity: more than satisfactory level of surgical conditions and the fact that the mother is able...
Eligibility Criteria
Inclusion
- Cesarean delivery at term under spinal anesthesia
- American Society of Anesthesiologists (ASA) physical status \<3
- BMI\<40
Exclusion
- Spinal anesthesia with the dose different than 12.5mg of hyperbaric bupivacaine
- Local anesthetic other than hyperbaric bupivacaine used
- Failed spinal anesthesia
- Poor quality of anesthetic record - required data not available
Key Trial Info
Start Date :
September 18 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
November 30 2025
Estimated Enrollment :
140 Patients enrolled
Trial Details
Trial ID
NCT07197398
Start Date
September 18 2025
End Date
November 30 2025
Last Update
September 29 2025
Active Locations (1)
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1
Centre of Postgraduate Medical Education,Department of Anesthesia and Intensive Care
Warsaw, Poland, 01-813