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NCT03730753

Programmed Intermittent Epidural Bolus Versus Continuous Infusion in Labour Analgesia

Status unknown NA Last updated 30 November 2023
What this trial tests

NA trial testing Programmed intermittent epidural bolus in Labor Pain in 200 participants. Status unknown.

Timeline
1 June 2019
Primary endpoint
30 June 2025
30 June 2025

Quick facts

Lead sponsorUniversité de Sherbrooke
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment200
Start date1 June 2019
Primary completion30 June 2025
Estimated completion30 June 2025
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Université de Sherbrooke — full company profile →

Who can join

18 and older, female only, with Labor Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to establish if programmed intermittent epidural bolus combined to patient controlled analgesia in labour analgesia will lower the hourly bupivacaine consumption when compared to continuous infusion combined with patient controlled analgesia. The investigators' hypothesis is that the use of programmed intermittent epidural bolus will lower the hourly bupivacaine consumption.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Programmed intermittent epidural bolus

Trials testing the same drug.

Other recruiting trials for Labor Pain

Currently open trials in the same condition.

Other Université de Sherbrooke trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03730753.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing