Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced

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.

See also
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Completed	`NCT05512065` - Changes in Velocimetric Indices of Uterine and Umbilical Arteries Before and After Combined Spinal-epidural Analgesia in Laboring Women	N/A
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Active, not recruiting	`NCT02271100` - Assessment of the Use of Ultrasound for Epidural Catheter Placement and Comparison With Palpation Technique	N/A
Completed	`NCT02926469` - Virtual Reality Analgesia in Labor: The VRAIL Pilot Study	N/A
Completed	`NCT03712735` - Programmed Intermittent Epidural Bolus For Laboring Obstetrical Women	Phase 4
Not yet recruiting	`NCT05565274` - Outcome of Combined Tramadol and Paracetamol Versus Pentazocine as Labour Analgesia Among Parturients	N/A
Recruiting	`NCT01708668` - The Effects of Intermittent Epidural Bolus on Fever During Labor Analgesia	N/A
Recruiting	`NCT02575677` - Oxycodone in Treatment of Early Labour Pain Efficacy and Safety

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

Spinal Fentanyl or Epidural Analgesia in the Early First Phase of Induced Labor

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms