CompletedPhase 4

Truncal Ultrasound Guided Regional Anesthesia for Implantation and Revision of Automatic Implantable Cardioverter Defibrillators (AICDs) and Pacemakers in Pediatric Patients

United States19 participantsStarted 2020-10-01

Plain-language summary

The purpose of this study is to determine the efficacy and safety of truncal blocks for pacemaker and Automatic Implantable Cardioverter Defibrillator implantation in children and to prospectively evaluate whether there is a decrease in amount of narcotic medications need and track complications.

Who can participate

Age range0 Years – 17 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients undergoing implantation or revision of pacemaker or AICD in the pediatric cath lab Exclusion Criteria: * parent or patient refusal * use of narcotic medications prior to procedure

What they're measuring

Total Narcotic Dose in Milligram Morphine Equivalents (MME) Per Kilogram

Timeframe: From 24 hours after procedure to 48 hours after procedure

Total Narcotic Dose in Milligram Morphine Equivalents (MME) Per Kilogram

Timeframe: up to 24 hours after procedure

Trial details

NCT IDNCT04184349

SponsorThe University of Texas Health Science Center, Houston

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-06-09

Results submitted2025-03-21

View on ClinicalTrials.gov More Analgesia After Pacemaker trials