Status:
UNKNOWN
Prediction of Post-Cesarean Section Pain
Lead Sponsor:
University of Washington
Conditions:
Postoperative Pain
Eligibility:
FEMALE
18-50 years
Brief Summary
The purpose of this study is to determine if dynamic psychophysical testing along with genetic screening will allow to identify pre-operatively women who will suffer severe acute pain post-operatively...
Eligibility Criteria
Inclusion
- Women age 18-50 scheduled for an elective cesarean section (1st or 2nd cesarean section)
Exclusion
- Women who:
- have taken opioids, acetaminophen, or NSAIDs 48 hrs prior to psychophysical testing
- have had more than two previous cesarean sections
- have a vertical abdominal incision from a prior cesarean section
- are non-English speaking
- have mental health issues
- have a failure of spinal anesthetic and require conversion to general anesthesia
- have a vertical uterine incision performed during ongoing cesarean section
- have a previous vertical uterine scar discovered during ongoing cesarean section
Key Trial Info
Start Date :
November 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
November 1 2013
Estimated Enrollment :
800 Patients enrolled
Trial Details
Trial ID
NCT00799162
Start Date
November 1 2008
End Date
November 1 2013
Last Update
September 26 2011
Active Locations (5)
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1
Stanford University
Stanford, California, United States, 94305
2
University of Washington
Seattle, Washington, United States, 98195
3
St. Luc Hospital, University Catholic of Louvain
Brussels, Brussels Capital, Belgium, 1200
4
Hospital e Maternidade Santa Joana
São Paulo, São Paulo, Brazil, 04103-080