NCT06085027

Comparison of the Epifaith® Syringe With the Plastic Syringe

Compare the Epifaith® Syringe With the Plastic Syringe for Identification of the Epidural Space in Parturients: A Prospective Randomized Control Study

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 300 (estimated)
• Sponsor: Chang Gung Memorial Hospital · Academic / Other
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: Accepted

Summary

The goal of this clinical trial is to compare the efficiency of identifying epidural space with either the Epifaith® syringe or the plastic syringe in parturients. The main questions it aims to answer are: * Whether it consume less time identifying epidural space with the Epifaith® syringe * Whether the usage of the Epifaith® syringe decrease the complication rate and failure of labor analgesia Participants will receive labor analgesia either with the Epifaith® syringe or the plastic syringe conducted by experienced resident doctors.

Conditions

• Epidural; Anesthesia, Headache
• Analgesia

Interventions

Type	Name	Description
PROCEDURE	Labor analgesia	Perform epidrual analgesia for parturients between 18 to 45 year-old

Timeline

• Start date: 2023-10-01
• Primary completion: 2024-07-01
• Completion: 2024-10-01
• First posted: 2023-10-16
• Last updated: 2023-10-16