Clinical Trials Directory

Trials / Completed

CompletedNCT04716660

Changes in Sensory Block Level During a Programmed Intermittent Epidural Bolus Regimen for Labor Analgesia: an Observational Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
34 (actual)
Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital · Academic / Other
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers

Summary

Epidural analgesia is widely used for managing pain during labor. The programmed intermittent epidural bolus (PIEB) technique has been shown to produce less consumption of local anesthetics, better sensory block, less motor block, and increased maternal satisfaction than other epidural analgesia techniques. Despite all benefits from PIEB, such practice has been associated with high sensory block levels. Therefore, assessment of the sensory block level is an essential component of clinical safety. The lack of a standardized technique and timing to assess the sensory block level can lead to inappropriate management. The purpose of this study is to investigate the changes in block level over time, during cycles of a PIEB regimen. The investigators hypothesize that these levels will be highest soon after the PIEB bolus and lowest preceding the subsequent PIEB bolus. The investigators also want to investigate a possible correlation between these changes in sensory block levels and motor block, pain scores, and rescue bolus of local anesthetics.

Conditions

Interventions

TypeNameDescription
OTHERSensory block level checkPatients will have their sensory block level checked multiple times following administration of their epidural bolus for labor analgesia.

Timeline

Start date
2021-02-02
Primary completion
2021-08-09
Completion
2021-08-09
First posted
2021-01-20
Last updated
2021-09-21

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT04716660. Inclusion in this directory is not an endorsement.