Trials / Terminated
TerminatedNCT03566342
Optimal Regimen of Patient-controlled Epidural Analgesia in Laboring Patients
Optimal Regimen of Patient-controlled Epidural Analgesia in Laboring Patients Receiving Combined Spinal and Epidural Analgesia (CSE)
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 145 (actual)
- Sponsor
- Maimonides Medical Center · Academic / Other
- Sex
- Female
- Age
- 16 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
To test the efficacy of different recipes of epidural infusions used for providing pain relief during labor in parturients.
Detailed 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.
Conditions
Timeline
- Start date
- 2007-08-01
- Primary completion
- 2015-07-01
- Completion
- 2015-07-01
- First posted
- 2018-06-25
- Last updated
- 2018-06-25
Source: ClinicalTrials.gov record NCT03566342. Inclusion in this directory is not an endorsement.