46 Participants NeededMy employer runs this trial

Postoperative Pacing for Heart Surgery

(POSTPACE Trial)

RG
JH
Overseen ByJeff Hong, MD
Age: < 18
Sex: Any
Trial Phase: Academic
Sponsor: Robert G. Webster, MD, MPH
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The goal of this study is to determine whether temporarily increasing a child's heart rate after heart surgery can improve blood flow and oxygen supply to the body's tissues. The study will compare temporary atrial pacing at 10 and 20 beats per minute above the child's natural heart rate with the child's natural heart rate without pacing.

Participants will be randomly assigned to one of two schedules for these pacing approaches. Each pacing approach has previously been used as part of routine care after heart surgery. The study will test whether temporarily increasing the heart rate improves blood flow and oxygen supply during the first 10 hours after surgery.

Who Is on the Research Team?

RG

Robert G Webster, MD, MPH

Principal Investigator

Ann & Robert H Lurie Children's Hospital of Chicago

Are You a Good Fit for This Trial?

This trial is for children who have just had congenital heart surgery. It excludes those with conditions that would make temporary pacing unsafe or not possible, but specific exclusions are not listed.

Inclusion Criteria

I am scheduled to be admitted to the CICU after my surgery.
I am younger than 12 years old, ideally under 12 months.
My child is between 13 months and 12 years old, depending on study needs.
See 2 more

Exclusion Criteria

Arterial pH less than 7.10
Junctional or ventricular rhythm at baseline
Category 2 and category 3 patients on the pulmonary artery reconstruction (PAR) program
See 7 more

What Are the Treatments Tested in This Trial?

Interventions

  • Temporary Atrial Pacing

Trial Overview

The study tests if temporarily increasing a child's heart rate using atrial pacing after heart surgery improves blood flow and oxygen delivery compared to no pacing. Children are randomly assigned to different pacing schedules during the first 10 hours after surgery.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Group 2: +20 bpm, +10 bpm, no pacingExperimental Treatment1 Intervention
Group II: Group 1: No pacing, +20 bpm, +10 bpmExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Robert G. Webster, MD, MPH

Lead Sponsor

Ann & Robert H Lurie Children's Hospital of Chicago

Collaborator

Trials
275
Recruited
5,182,000+