Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
  • Induced; Birth
  • Labor Pain
Type
Interventional
Phase
Phase 4
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: 60 parturients randomized to two different treatment arms (30 in each group)Masking: Triple (Participant, Investigator, Outcomes Assessor)Masking Description: The parturient and the midwife as well as the researcher doing the interview for analgesia will be masked. The anesthesiologist performing either spinal fentanyl administration or epidural analgesia will not be maskedPrimary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 50 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04645823
Collaborators
Not Provided
Investigators
Principal Investigator: Antti J Vaananen, MD PhD HUCH, Women's hospital/dept of anesthesia