Status:
COMPLETED
Analgesia in the Second Stage of Labour
Lead Sponsor:
Oslo University Hospital
Conditions:
Childbirth Experience
Urinary Retention
Eligibility:
FEMALE
18+ years
Brief Summary
This study investigates efficacy, safety and childbirth experience in women receiving pudendal block during the final stage of delivery. It is an observational study and half of included primarous wom...
Detailed Description
Pudendal block is used when there is a need to alleviate pain in the final stage of labour: * From fully dilated cervix to delivery of the child. * Associated with pain as the foetus rotates and desc...
Eligibility Criteria
Inclusion
- Norwegian-speaking/reading
- Primiparity
- Single pregnancy
- Vaginal birth
- Cephalic presentation
- ≥37+0
- Age ≥18 years
Exclusion
- Transferre from midwifery-led birth unit
- Allergy to local anaesthesia
- Not valid data on pudendal block
Key Trial Info
Start Date :
January 1 2017
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 31 2019
Estimated Enrollment :
1007 Patients enrolled
Trial Details
Trial ID
NCT04391075
Start Date
January 1 2017
End Date
May 31 2019
Last Update
May 19 2020
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.