Superiority of Epidural Placement Technique Using EpiFaith Syringe

Status Withdrawn

Clinical Trial Summary

The aim of this study is to evaluate the impact of EpiFaith® syringe on the establishment of successful epidural labor analgesia, change of elapsed time for identification of epidural space, and learning curve of CA-1 residents.

Clinical Trial Description

We hypothesize that EpiFaith® syringe, in comparison with conventional glass syringe, will result in a similar overall success rate for catheter placement, but with a larger reduction in change of elapsed time for identification of epidural space and catheter placement of each practitioner. Moreover, we hypothesize that the cumulative learning summary curve using EpiFaith® syringe will be higher than conventional glass syringe in resident trainees, which will show the possible value of EpiFaith® syringe for teaching and learning obstetric epidural anesthesia. ;

Study Design

Related Conditions & MeSH terms

Anesthesia

Clinical Trial Details

NCT number	NCT04793373
Study type	Interventional
Source	Harvard Medical School (HMS and HSDM)
Contact
Status	Withdrawn
Phase	N/A
Start date	May 15, 2022
Completion date	June 30, 2026

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