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NCT05260320 · ClinicalTrials.gov registry record · NA

Anesthetic Optimization in Pediatric LeFort Surgeries

A NA study of Pain, Postoperative and Le Fort, sponsored by Johns Hopkins University.

Recruiting
Registry status
NA
Development phase
50
Enrollment target
1
Study location

NCT05260320 is a NA study of Pain, Postoperative and Le Fort that is actively recruiting participants, run by Johns Hopkins University. The registered enrollment target is 50 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05260320, a NA study of Pain, Postoperative and Le Fort, is actively recruiting participants, sponsored by Johns Hopkins University.

RECRUITING
Registry status
NA
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

This study will propose and evaluate a standardized LeFort osteotomy anesthetic protocol for pediatric patients at Johns Hopkins Hospital. There are two cohorts to this study: a prospective cohort who will receive the study anesthesia protocol and a historical cohort that received standard of care. The investigators hope this will help to minimize unnecessary postoperative pain management, inpatient stay, and long-term morbidity and mortality in these patients.

Conditions Studied

Pain, Postoperative Le Fort

Interventions

  • OTHER Standardized Anesthetic Course from Premedication to Induction

Study Locations (1)

Maryland

  • Johns Hopkins Hospital - Baltimore

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-05-02
Est. Completion 2027-07
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

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What the Registry Record Tells You About NCT05260320

The ClinicalTrials.gov registry entry for NCT05260320 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (82% lower). The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 1 intervention - of which Standardized Anesthetic Course from Premedication to Induction is the first listed.

NCT05260320 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT05260320 about?

NCT05260320 is a clinical study titled "Anesthetic Optimization in Pediatric LeFort Surgeries". This study will propose and evaluate a standardized LeFort osteotomy anesthetic protocol for pediatric patients at Johns Hopkins Hospital. There are two cohorts to this study: a prospective cohort who will receive the study anesthesia protocol and a historical cohort that received standard of care. ...

What is the current status of trial NCT05260320?

This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2025-05-02. Estimated completion is 2027-07.

What conditions does trial NCT05260320 study?

This clinical trial studies the following conditions: Pain, Postoperative, Le Fort.

What interventions are being tested in trial NCT05260320?

The interventions under investigation include: Standardized Anesthetic Course from Premedication to Induction (OTHER).

Who is sponsoring clinical trial NCT05260320?

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

Where is trial NCT05260320 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.