Status:
COMPLETED
Comparison of Loss of Resistance Techniques
Lead Sponsor:
Wake Forest University Health Sciences
Conditions:
Pain Relief
Eligibility:
FEMALE
Phase:
PHASE2
Brief Summary
The purpose of this study is to determine whether there is a difference in success outcome of the combined spinal epidural labor analgesia between air versus saline when used to identify the epidural ...
Detailed Description
When the epidural needle is inserted initially, it is typically connected to a syringe filled with 2-3 ml or air or saline. This is used to help identify the placement of the epidural needle. Both air...
Eligibility Criteria
Inclusion
- Pregnant females weighing less than or equal to 250 lbs
- Request for neuraxial labor analgesia
Exclusion
- ASA physical status greater than II
Key Trial Info
Start Date :
July 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2008
Estimated Enrollment :
356 Patients enrolled
Trial Details
Trial ID
NCT00638274
Start Date
July 1 2005
End Date
May 1 2008
Last Update
November 9 2018
Active Locations (1)
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1
Forsyth Medical Center
Winston-Salem, North Carolina, United States, 27103