Trials / Completed
CompletedNCT03712735
Programmed Intermittent Epidural Bolus For Laboring Obstetrical Women
Effect of Programmed Intermittent Epidural Bolus Delivery Rate on the Quality of Labour Analgesia: A Randomized Clinical Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 390 (actual)
- Sponsor
- University of British Columbia · Academic / Other
- Sex
- Female
- Age
- 19 Years
- Healthy volunteers
- Accepted
Summary
Comparison of three programmed intermittent epidural bolus (PIEB) pump settings for maintenance of labour analgesia.
Detailed description
The optimal PIEB and patient controlled epidural administered (PCEA) bolus settings are still unknown. Therefore, in this study, the investigators aim to compare analgesia outcomes both high and low PIEB flow rate settings.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine 0.08% - fentanyl 2mcg | In each arm, bupivacaine and fentanyl are being delivered at different intervals and rates for the maintenance of labor analgesia. |
Timeline
- Start date
- 2018-10-23
- Primary completion
- 2021-03-02
- Completion
- 2021-03-02
- First posted
- 2018-10-19
- Last updated
- 2021-04-26
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT03712735. Inclusion in this directory is not an endorsement.