Status:
COMPLETED
The Association Between Decreasing Labor Analgesia Epidural Infusion and Forceps Delivery
Lead Sponsor:
Northwestern University
Conditions:
Labor Pain
Pregnancy
Eligibility:
FEMALE
18-60 years
Brief 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...
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 prov...
Eligibility Criteria
Inclusion
- Singletons
- Viable fetal vaginal deliveries between January 2004-October 2005
Exclusion
- Outside specified time frame
- Multiparity
- Fetal demise
Key Trial Info
Start Date :
January 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
March 1 2006
Estimated Enrollment :
2162 Patients enrolled
Trial Details
Trial ID
NCT00443560
Start Date
January 1 2006
End Date
March 1 2006
Last Update
April 14 2014
Active Locations (1)
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1
Northwestern University
Chicago, Illinois, United States, 60611