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A Comparison Study Of Two Different Techniques For Identifying The Epidural Space In Parturients In Labour

NCT01574391 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2015-04-14

No results posted yet for this study

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.

Conditions

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

Interventions

DEVICE

Epidrum

Epidrum is used

Sponsors & Collaborators

  • National Maternity Hospital, Ireland

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-07-31
Completion
2012-08-31

Countries

  • Ireland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01574391 on ClinicalTrials.gov