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Clinical Trial Summary

The purpose of this study is to determine whether the use of the Epidrum device to identify the epidural space in labouring parturients reduces morbidity, when compared to standard loss of resistance techniques.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Labouring Parturients Requiring/Requesting Epidural Analgesia as Part of Their Peri-partum Care

NCT number NCT01574391
Study type Interventional
Source National Maternity Hospital, Ireland
Contact
Status Completed
Phase N/A
Start date March 2012
Completion date August 2012