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NCT04826484 · ClinicalTrials.gov registry record · Phase 3

Opioid Reduction Initiative During Outpatient Pediatric Urologic Procedures Using Exparel

A Phase 3 study, sponsored by Johns Hopkins University.

Terminated
Registry status
Phase 3
Development phase
104
Enrollment target

NCT04826484: Clinical Trial Phase 3 study, sponsored by Johns Hopkins University.

NCT04826484 is a Phase 3 study that was terminated before completion, run by Johns Hopkins University. The registered enrollment target is 104 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04826484, a Phase 3 study, was terminated before completion, sponsored by Johns Hopkins University.

TERMINATED
Registry status
Phase 3
Development phase
104 participants
Enrollment target

Study Summary

This study aims to evaluate the utility of long-acting liposomal bupivacaine (Exparel®) in improving pain scores and reducing narcotic pain requirements in pediatric patients following minor urologic procedures.

Primary Outcome

Percentage of patients who are opiate-free at 48 hours postoperatively.

Interventions

  • DRUG Bupivacaine Hydrochloride
  • DRUG Exparel 133 miligrams per 10 milliliter injection

Trial Details

FieldValue
Enrollment Target 104 participants
Start Date 2021-10-01
Est. Completion 2023-04-26
Phase Phase 3
Johns Hopkins University

1,448 total trials

Why NCT04826484 stopped before completion

NCT04826484 is an interventional study that assigns participants to a tested intervention. The registered 104 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (87% lower).

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

NCT04826484 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04826484 about?

NCT04826484 is a clinical study titled "Opioid Reduction Initiative During Outpatient Pediatric Urologic Procedures Using Exparel". This study aims to evaluate the utility of long-acting liposomal bupivacaine (Exparel®) in improving pain scores and reducing narcotic pain requirements in pediatric patients following minor urologic procedures.

What is the current status of trial NCT04826484?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 104 participants. The study started on 2021-10-01. Estimated completion is 2023-04-26.

What interventions are being tested in trial NCT04826484?

The interventions under investigation include: Bupivacaine Hydrochloride (DRUG), Exparel 133 miligrams per 10 milliliter injection (DRUG).

Who is sponsoring clinical trial NCT04826484?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04826484's enrollment target sits among peer trials

104 1671st of 2000 higher than 327 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT04826484, the US trial registry maintained by the National Library of Medicine. NCT04826484 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.