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Keep this study
Lead
Wake Forest University Health Sciences
This study is randomizing patients into 2 different groups and seeing if by altering our pain management with this group of patients their acute 24 hour evoked pain is less than anticipated; and the incidence of persistent pain and depression when contacted 2 months after delivery is decreased. This study is designed to see if these additional interventions would prove effective for patients at risk of having high pain level after cesarean surgery.
Age
18–45
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
elective cesarean section
age \>/= 18 years old
not allergic proposed study medications
predicted to experience high pain postop based on preoperative evaluation
You may not be if
allergy to study medications
known hepatic disease
weight \> 300 lbs
Clareo Health | High Pain Intervention in Cesarean Sections
