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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04645823
Study type Interventional
Source Women's Hospital HUS
Contact
Status Completed
Phase Phase 4
Start date March 26, 2021
Completion date May 19, 2023

See also
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