Intermittent Bolus vs Continuous Infusion Via ESP Catheters RCT

Status Recruiting

Clinical Trial Summary

The purpose of this prospective randomized controlled trial is to compare the effectiveness of two different delivery methods for postoperative pain management following cardiac surgery requiring median sternotomy: intermittent programmed LA bolus versus continuous LA infusion through ESP catheters. Effectiveness of analgesia will be assessed based on the subjects' NRS pain scores and opioid consumption. The primary outcome measure will be the patients' opioid consumption over the course of the 72 hours following surgery. Secondary outcomes measures that will be evaluated include NRS pain scores, intensive care unit (ICU) length of stay, and time to first dose of antiemetic in the postoperative period. It is hypothesized that the use of intermittent programmed LA boluses will provide better analgesia compared to continuous LA infusion through ESP catheters. The findings of this study will provide guidance regarding the optimal method of delivery for postoperative pain management in patients following cardiac surgery.

Clinical Trial Description

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05642416
Study type	Interventional
Source	Henry Ford Health System
Contact	Katherine Nowak, PhD
Phone	313-771-7128
Email	knowak2@hfhs.org
Status	Recruiting
Phase	Phase 4
Start date	October 15, 2022
Completion date	November 30, 2024

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