Clinical Trials Directory

Trials / Completed

CompletedNCT02793596

Reliability of Waveform Analysis as an Adjunct to Loss of Resistance for Obstetrical Epidural Blocks

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
McGill University Health Centre/Research Institute of the McGill University Health Centre · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

In this study, we will set out to confirm the reliability of epidural waveform analysis (EWA) as an adjunct to loss of resistance for obstetrical epidural blocks.

Detailed description

After loss of resistance, 5 mL of normal saline will be injected through the epidural needle; the latter will then be connected to a pressure transducer (leveled with the heart) using a rigid tubing. A pressure recording of the epidural waveform will be saved for future assessment by a blinded observer. After the recording of the waveform, the rigid tubing will be disconnected from the epidural needle. A 4 mL bolus of lidocaine 2% with epinephrine 5 µg/mL will be injected through the latter. An epidural catheter will be advanced 3-4 cm past the tip of the needle inside the epidural space. The needle will then be removed and the catheter secured to the skin in the usual fashion. Fifteen minutes after the injection of the local anesthetic bolus, a blinded observer will apply ice to the T1-L5 dermatomes and assess the epidural block.

Conditions

Interventions

TypeNameDescription
OTHERObstetrical patientsEpidural waveform analysis as a confirmation of loss of Resistance

Timeline

Start date
2016-08-01
Primary completion
2016-11-01
First posted
2016-06-08
Last updated
2017-03-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02793596. Inclusion in this directory is not an endorsement.