Trials / Not Yet Recruiting
Not Yet RecruitingNCT06094946
Parturient Satisfaction With Epidural Analgesia by PCEA or Manual Boluses
Parturient Satisfaction With Epidural Analgesia During Parturient Controlled Pump
- Status
- Not Yet Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (estimated)
- Sponsor
- Women's Hospital HUS · Academic / Other
- Sex
- Female
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
Those prospective parturients that express that they may want an epidural labour analgesia for their delivery will be informed about the possibility to choose between a pump driven epidural or midwife administered intermittent boluses.
Detailed description
The purpose is to compare parturient and midwife satisfaction with the epidural labour analgesia when epidural analgesia is maintained by an epidural bolus pump (automated mandatory boluses with patient controlled boluses without background infusion) or midwife administered on-demand boluses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine Hydrocloride | 1 mg/ml |
| DRUG | Fentanyl Citrate | 2.5 micrograms/ml |
Timeline
- Start date
- 2024-12-01
- Primary completion
- 2025-02-01
- Completion
- 2025-02-01
- First posted
- 2023-10-23
- Last updated
- 2024-04-24
Locations
1 site across 1 country: Finland
Source: ClinicalTrials.gov record NCT06094946. Inclusion in this directory is not an endorsement.