Pain Relief Clinical Trial
Official title:
Comparison of Loss of Resistance Technique With Air Versus Saline to Identify Epidural Space for Combined Spinal Epidural Labor Analgesia
Verified date | October 2018 |
Source | Wake Forest University Health Sciences |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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 space.
Status | Completed |
Enrollment | 356 |
Est. completion date | May 2008 |
Est. primary completion date | May 2008 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - Pregnant females weighing less than or equal to 250 lbs - Request for neuraxial labor analgesia Exclusion Criteria: - ASA physical status greater than II |
Country | Name | City | State |
---|---|---|---|
United States | Forsyth Medical Center | Winston-Salem | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Wake Forest University Health Sciences |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Success of Spinal Labor Analgesia From Combined Spinal Epidural | Number of participants that had successful spinal labor analgesia in each group. | 24 hours | |
Secondary | Number of Participants With Failed Epidural Catheters | Number of Participants with Failed Epidural Catheters and that had to be replaced at any time measured from the time of the catheter is placed until the time of delivery. | 24 hours |
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