Continuous vs Intermittent Ketorolac for Pediatric Heart Surgery

Continuous vs Intermittent Ketorolac for Pain Control in Peds CV Surgery

Recruiting Phase 4 Interventional Study
Congenital Heart Disease in Children
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
3 Months – 59 Months
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Supportive Care
Participants needed
166 (estimated)
Sponsor
Phoenix Children's Hospital · Other
Who this trial is looking for

This trial is looking for children aged 3 months to 4 years who have had heart surgery. Participants will receive either continuous or intermittent doses of ketorolac to manage pain after their procedure.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am between 3 months and 4 years old.
  • I have had heart surgery and am in the CVICU.
  • I can start ketorolac within 12-24 hours after my surgery.
  • My doctor thinks ketorolac is the right pain relief for me.

You may not be able to join if

  • I have acute kidney injury.
  • I am allergic to ketorolac or any NSAID medications.
  • I need mechanical support like ECMO within 48 hours after surgery.
  • I have had a heart transplant.
  • I have significant bleeding.
  • I have known kidney problems before my surgery.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

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About This Trial

The proposed study will be a prospective, randomized, double blind, placebo controlled trial to compare the use of a continuous infusion versus intermittent ketorolac on postoperative patients in the pediatric cardiovascular ICU. We intend to determine if the continuous infusion leads to a decreased utilization of opiates when compared to intermittent ketorolac.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. All patients aged 3 months to 4 years 11months admitted post operatively to the CVICU during the time period in which the study will be ongoing 2. Initiation of study medication within the first 12-24 hours post-operatively 3. The cardiovascular attending of record after revi…
Contacts

Kevin Engelhardt, MD

6029333366

kengelhardt@phoenixchildrens.com

CONTACT

Samantha Stack, BS

6029330607

sstack@phoenixchildrens.com

CONTACT