Status:
UNKNOWN
Effect of Higher Volume and Lower Dose on Analgesic Quality During Labor Analgesia With Dural Puncture Epidural
Lead Sponsor:
Ataturk University
Conditions:
Analgesia
Eligibility:
FEMALE
20-45 years
Phase:
NA
Brief Summary
It is aimed in this study to compare the effect of using local anaesthetics in a higher volume and lower dose on the total anesthetic consumption and quality of labor analgesia with dural puncture epi...
Detailed 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 obtain...
Eligibility Criteria
Inclusion
- Healthy nulliparous women
- American Society of Anaesthesiology Score of II
- During active labor
- At weeks 37-42.
- Singlet vertex presentation
- Cervical dilation \<5 cm at the request of labor analgesia
- VAS score \>40
Exclusion
- Age \<20 or \>45,
- Morbid obesity
- Presence of pregnancy-related comorbidities (e.g: gestational diebetes, gestational hypertension and preeclampsia)
- History of drug abuse
- Contrindication for neuraxial blocks
- Conditions that increase the risk of need for cesarean section (e.g. placenta previa, uterus abnormalities or surgeries)
- Diagnosed fetal abnormalities
- Cases where dura gets punctured unintendedly with the epiduralneedle
- Cases where flow of cerebrospinal fluid (CSF) is not observed after dural puncture
- Cases where a cesarean section is performed at any stage of labor
- Cases where labor is completed in 1 hour from the start of analgesia procedure.
Key Trial Info
Start Date :
November 20 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
October 1 2025
Estimated Enrollment :
54 Patients enrolled
Trial Details
Trial ID
NCT06156709
Start Date
November 20 2023
End Date
October 1 2025
Last Update
December 5 2023
Active Locations (1)
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1
Atatürk University
Erzurum, Turkey (Türkiye)