Viewing Study NCT03712735


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Study NCT ID: NCT03712735
Status: COMPLETED
Last Update Posted: 2021-04-26
First Post: 2018-10-17
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Programmed Intermittent Epidural Bolus For Laboring Obstetrical Women
Sponsor: University of British Columbia
Organization:

Study Overview

Official Title: Effect of Programmed Intermittent Epidural Bolus Delivery Rate on the Quality of Labour Analgesia: A Randomized Clinical Trial
Status: COMPLETED
Status Verified Date: 2021-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Comparison of three programmed intermittent epidural bolus (PIEB) pump settings for maintenance of labour analgesia.
Detailed Description: The optimal PIEB and patient controlled epidural administered (PCEA) bolus settings are still unknown. Therefore, in this study, the investigators aim to compare analgesia outcomes both high and low PIEB flow rate settings.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: