Clinical Trials Directory

Trials / Completed

CompletedNCT00443560

The Association Between Decreasing Labor Analgesia Epidural Infusion and Forceps Delivery

A Retrospective Case-controlled Study of the Association Between Request to Discontinue Second Stage Labor Epidural Analgesia and Risk of Instrumental Vaginal Delivery

Status
Completed
Phase
Study type
Observational
Enrollment
2,162 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

The objective of this study will be to compare epidural infusion management, specifically looking at infusion rate changes, in patients who receive forceps deliveries versus normal spontaneous vaginal deliveries. We will match patients based on time and date of delivery, as well as parity, in order to eliminate these variables as potential con-founders. We hypothesize patients who require a decrease in their basal labor analgesia epidural infusion rate will have an increased incidence of forceps delivery.

Detailed description

The obstetrical anesthesia database will be queried for all forceps deliveries between the dates of January 2004-October 2005. To minimize the influence of different anesthetic and obstetric care providers, the control group consisted of parturients who has spontaneous vaginal deliveries (SVD) in the same 24 hour period who were case-matched for gravidity and parity. Parturients with twin deliveries and fetal demise were not selected for either group. The database will be queried for the following: maternal age, parity, gestational age, type of analgesia, changes in epidural infusion rate and/or concentration, and supplemental bolus doses of local anesthesia. The data will be stripped of identification by the database manager and entered into a secured computer which is password protected and maintained in the Department of Anesthesiology. The primary endpoint is to evaluate if decreasing the epidural infusion rate was associated with a forceps delivery.

Conditions

Interventions

TypeNameDescription
OTHERCase controlled analysis of epidural labor analgesia patternsA retrospective study utilizing the Obstetric Anesthesiology Database to identify parturients who received neuraxial labor analgesia initiated with a combined spinal epidural (CSE) technique and maintained with a continuous epidural infusion with patient controlled epidural analgesia boluses

Timeline

Start date
2006-01-01
Primary completion
2006-03-01
Completion
2006-03-01
First posted
2007-03-06
Last updated
2014-04-14
Results posted
2011-07-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00443560. Inclusion in this directory is not an endorsement.