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

NCT04645823 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-04-24

No results posted yet for this study

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

  • Labor Pain
  • Induced; Birth

Interventions

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

Sponsors & Collaborators

  • Women's Hospital HUS

    lead OTHER

Principal Investigators

  • Antti J Vaananen, MD PhD · HUCH, Women's hospital/dept of anesthesia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-26
Primary Completion
2023-05-19
Completion
2023-05-19

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04645823 on ClinicalTrials.gov