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NCT04184349 · ClinicalTrials.gov registry record · Phase 4

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

A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.

Completed
Registry status
Phase 4
Development phase
19
Enrollment target

NCT04184349: Completed Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.

NCT04184349 is a Phase 4 study that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 19 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04184349, a Phase 4 study, has completed, sponsored by The University of Texas Health Science Center, Houston.

COMPLETED
Registry status
Phase 4
Development phase
19 participants
Enrollment target

Study 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.

Interventions

  • DRUG LA group
  • DRUG B Group

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2020-10-01
Est. Completion 2022-06-09
Phase Phase 4

What the finished NCT04184349 record still lists

NCT04184349 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which LA group is the first listed.

NCT04184349 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04184349 about?

NCT04184349 is a clinical study titled "Truncal Ultrasound Guided Regional Anesthesia for Implantation and Revision of Automatic Implantable Cardioverter Defibrillators (AICDs) and Pacemakers in Pediatric Patients". 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.

What is the current status of trial NCT04184349?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 19 participants. The study started on 2020-10-01. Estimated completion is 2022-06-09.

What interventions are being tested in trial NCT04184349?

The interventions under investigation include: LA group (DRUG), B Group (DRUG).

Who is sponsoring clinical trial NCT04184349?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04184349's enrollment target sits among peer trials

19 1834th of 2000 higher than 159 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04184349, the US trial registry maintained by the National Library of Medicine. NCT04184349 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.