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Clinical Trial Summary

It is aimed in this study to compare the effect of changing the interval time for programmed auto boluses of local anaesthetics on the total anesthetic consumption and quality of labor analgesia with dural puncture epidural technique.


Clinical Trial Description

This study will be conducted as a prospective randomized, controlled, double-blind trial following the approval of the ethical committee at Atatürk University Medical Faculty Hospital and after obtaining written consent from the participating patients. The study will include pregnant women aged 20 to 45 with American Society of Anesthesiologists (ASA) II classification, full-term, nulliparous and singleton pregnancies. Using a randomisation procedure, the participants will be allocated into two equal groups: Group I and Group II. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06329713
Study type Interventional
Source Ataturk University
Contact Aysenur Dostbil
Phone +905333677796
Email adostbil@hotmail.com
Status Recruiting
Phase N/A
Start date March 15, 2024
Completion date August 1, 2025

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