Trials / Completed
CompletedNCT01741259
A Comparison of Meperidine for Post-Cesarean Analgesia: Bolus Versus Infusion and Bolus
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 273 (actual)
- Sponsor
- Mercy Research · Academic / Other
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Accepted
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.
Detailed description
The objective of this study is to compare the efficacy, patient satisfaction, and incidence of side effects of meperidine patient-controlled epidural analgesia (PCEA) with and without a basal infusion for post-cesarean section analgesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Meperidine |
Timeline
- Start date
- 2013-08-01
- Primary completion
- 2015-04-01
- Completion
- 2015-04-01
- First posted
- 2012-12-04
- Last updated
- 2017-10-25
- Results posted
- 2017-10-25
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01741259. Inclusion in this directory is not an endorsement.