Trials / Completed
CompletedNCT04645823
Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced Labor
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Women's Hospital HUS · Academic / Other
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
A total of 60 parturients undergoing induction of labour will be consented to participate in the study where they will be randomized to receive either spinal fentanyl (20 µg) or epidural analgesia (fentanyl 100µg and lidocaine 80 mg). They will be monitored for the development of analgesia for a duration of 30 minutes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Fentanyl Citrate | Fentanyl citrate 20 µg in 2 ml of saline injected into csf |
| DRUG | Lidocaine 1% Injectable Solution | Fentanyl citrate 100µg and lidocaine hydrochloride 80 mg in 10 ml volume |
| DRUG | Fentanyl Citrate | Fentanyl citrate 100µg and lidocaine hydrochloride 80 mg in 10 ml volume |
Timeline
- Start date
- 2021-03-26
- Primary completion
- 2023-05-19
- Completion
- 2023-05-19
- First posted
- 2020-11-27
- Last updated
- 2024-04-24
Locations
1 site across 1 country: Finland
Source: ClinicalTrials.gov record NCT04645823. Inclusion in this directory is not an endorsement.