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NCT06494904 · ClinicalTrials.gov registry record · Phase 3

Standard Versus High Dose ED-Initiated Buprenorphine Induction

A Phase 3 study of Opioid Use Disorder, sponsored by Yale University.

Recruiting
Registry status
Phase 3
Development phase
360
Enrollment target
5
Study locations

NCT06494904 is a Phase 3 study of Opioid Use Disorder that is actively recruiting participants, run by Yale University. The registered enrollment target is 360 participants, below the 4,655-participant average among 257 other Opioid Use Disorder trials with a reported enrollment target (92% lower). The trial reports 5 study locations across 4 states.

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The verdict

NCT06494904, a Phase 3 study of Opioid Use Disorder, is actively recruiting participants, sponsored by Yale University.

RECRUITING
Registry status
Phase 3
Development phase
360 participants
Enrollment target
5
Study locations

Study Summary

This study is a multisite double-blind, double-dummy, randomized clinical trial enrolling ED patients with untreated moderate to severe opioid use disorder (OUD) to compare Standard Dose Induction (SDI) and High Dose Induction (HDI) on rates of participation in OUD treatment within 10 days post randomization, and opioid withdrawal symptoms, opioid craving, and use of illicit and non-prescribed drugs.

Conditions Studied

Interventions

  • DRUG Buprenorphine

Study Locations (5)

California

  • Highland Hospital - Oakland
  • San Leandro Hospital - San Leandro

Maine

  • Maine Medical Center - Portland

New Jersey

  • Cooper University Hospital - Camden

Utah

  • University of Utah Hospital - Salt Lake City

Trial Details

FieldValue
Enrollment Target 360 participants
Start Date 2024-12-06
Est. Completion 2028-12
Phase Phase 3

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT06494904

The ClinicalTrials.gov registry entry for NCT06494904 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 360 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,655-participant average among 257 other Opioid Use Disorder trials with a reported enrollment target (92% lower). The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Opioid Use Disorder appearing as the primary indexed condition, and to 1 intervention - of which Buprenorphine is the first listed.

NCT06494904 reports 5 study locations spanning 4 distinct geographic areas - top geographies include California, Maine, New Jersey.

Frequently Asked Questions

What is clinical trial NCT06494904 about?

NCT06494904 is a clinical study titled "Standard Versus High Dose ED-Initiated Buprenorphine Induction". This study is a multisite double-blind, double-dummy, randomized clinical trial enrolling ED patients with untreated moderate to severe opioid use disorder (OUD) to compare Standard Dose Induction (SDI) and High Dose Induction (HDI) on rates of participation in OUD treatment within 10 days post rand...

What is the current status of trial NCT06494904?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 360 participants. The study started on 2024-12-06. Estimated completion is 2028-12.

What conditions does trial NCT06494904 study?

This clinical trial studies the following conditions: Opioid Use Disorder.

What interventions are being tested in trial NCT06494904?

The interventions under investigation include: Buprenorphine (DRUG).

Who is sponsoring clinical trial NCT06494904?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06494904 being conducted?

This trial has 5 study locations across California, Maine, New Jersey, Utah. 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.