NCT04012450

The Effects of Combined Spinal-epidural Anesthetics During Labor

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (estimated)
• Sponsor: Rambam Health Care Campus · Academic / Other
• Sex: Female
• Age: 18 Years – 40 Years
• Healthy volunteers: Not accepted

Summary

Women who fulfil the inclusion criteria and who intended to regional anesthesia will be randomized into the epidural anesthesia arm or to the spinal-epidural anesthesia arm. Sonographic evaluation of the flow in the uterine artery, umbilical artery, and middle cerebral artery will be documented to each patient prior and following the regional anesthesia.

Detailed description

Patients will receive information regarding the available anesthesia during labor that are available in the delivery room including regional and systemic. After receiving the patient informed consent for regional anesthesia (epidural or spinal-epidural), patients will be offered to participate in our study. After receiving the patients' informed consent for participating in the study, patients will be randomized to either the epidural anesthesia group or to the spinal-epidural anesthesia group. A doppler ultrasound will be performed on each patient prior to and following the regional anesthesia, the flow in the uterine artery, umbilical artery, and the middle cerebral artery of the fetus will be recorded. Demographic and obstetrical information will be collected from the patients' electronic files.

Conditions

• Anesthesia

Interventions

Type	Name	Description
PROCEDURE	Epidural anesthesia	Performing an epidural anesthesia
PROCEDURE	spina-epidural anesthesia	Performing a spina-epidural anesthesia

Timeline

• Start date: 2019-08-01
• Primary completion: 2021-08-31
• Completion: 2022-04-01
• First posted: 2019-07-09
• Last updated: 2019-07-09