Overview
A Comparison of Meperidine for Post-Cesarean Analgesia: Bolus Versus Infusion and Bolus
Status:
Completed
Completed
Trial end date:
2015-04-01
2015-04-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this study is to determine if epidural meperidine administered by patient-controlled bolus button is equivalent to a low dose infusion plus patient-controlled bolus.Phase:
N/AAccepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Mercy Research
St. John's Health System, MissouriTreatments:
Meperidine
Criteria
Inclusion Criteria are as follows:- Over the age of 18
- Undergoing non-urgent, non-emergent cesarean section at Mercy Hospital St. Louis
Exclusion Criteria:
- non-English speaking
- mentally disabled
- allergy to meperidine
- seizure disorder
- renal impairment defined as a serum creatinine >0.8 mg/dL or patients who give a
history of renal impairment
- fever greater than 101
- patients receiving low molecular weight heparin at any dose or unfractionated heparin
at doses greater than 5000 u subcutaneous twice daily
- pre-eclampsia requiring magnesium due to post-partum room assignment
- obstructive sleep apnea due to post-partum room assignment
- post-partum hemorrhage due to post-partum room assignment