Overview

A Comparison of Meperidine for Post-Cesarean Analgesia: Bolus Versus Infusion and Bolus

Status:
Completed
Trial end date:
2015-04-01
Target enrollment:
0
Participant gender:
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/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Mercy Research
St. John's Health System, Missouri
Treatments:
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