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Optimal Regimen of Patient-controlled Epidural Analgesia in Laboring Patients — PCEA  

LABOR PAIN Clinical Trial

Official title:
Optimal Regimen of Patient-controlled Epidural Analgesia in Laboring Patients Receiving Combined Spinal and Epidural Analgesia (CSE)

Clinical Trial Summary

To test the efficacy of different recipes of epidural infusions used for providing pain relief during labor in parturients.

Clinical Trial Description

In this prospective trial, the investigators would like to examine the efficacy of several different PCEA protocols in 250 parturients who receive CSE for labor pain. Any patient with failed epidural, delivery within 2 hours of epidural insertion, or Cesarean section will be excluded from the study. Each patient will be assigned to one of five groups (A - E), depending on the day of admission for delivery, excluding Friday and Saturday (observed religious holidays). Each group will have 50 patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03566342
Study type Observational [Patient Registry]
Source Maimonides Medical Center
Contact
Status Terminated
Phase
Start date August 2007
Completion date July 2015
View Details
See also
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