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COMPLETED
NCT05642416
PHASE4

Intermittent Bolus vs Continuous Infusion Via ESP Catheters RCT

Sponsor: Henry Ford Health System

View on ClinicalTrials.gov

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.

Official title: Intermittent Bolus Versus Continuous Infusion Erector Spinae Catheters for Median Sternotomy Incisions: A Prospective Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 90 Years

Study Type

INTERVENTIONAL

Enrollment

240

Start Date

2022-10-18

Completion Date

2024-12-23

Last Updated

2026-05-13

Healthy Volunteers

No

Interventions

DRUG

Continuous Infusion of ropivacaine

Continuous infusion of ropivacaine

DRUG

Intermittent bolus of ropivacaine

Intermittent bolus of ropivacaine

Locations (1)

Henry Ford Hospital

Detroit, Michigan, United States