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NCT06593093 · ClinicalTrials.gov registry record · Phase 1

A Bundled Intervention

A Phase 1 study of Opioid Use Disorder and Opioid Overdose, sponsored by University of Alabama at Birmingham.

Recruiting
Registry status
Phase 1
Development phase
190
Enrollment target
1
Study location

NCT06593093 is a Phase 1 study of Opioid Use Disorder and Opioid Overdose that is actively recruiting participants, run by University of Alabama at Birmingham. The registered enrollment target is 190 participants, below the 4,656-participant average among 257 other Opioid Use Disorder trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06593093, a Phase 1 study of Opioid Use Disorder and Opioid Overdose, is actively recruiting participants, sponsored by University of Alabama at Birmingham.

RECRUITING
Registry status
Phase 1
Development phase
190 participants
Enrollment target
1
Study location

Study Summary

Opioid overdose deaths have reached historically high records in the United States and are particularly concentrated among patients after emergency department (ED) discharge. Evidence-based treatment modules to reduce repeat opioid overdose and mortality are lacking in this patient population. A bundled intervention is proposed, including telehealth, peer support specialist, buprenorphine, and linkage for definitive care, that is designed to increase treatment uptake in this patient population post-ED discharge, reduce repeat opioid overdoses, and end overdose deaths.

Interventions

  • OTHER a bundled intervention
  • OTHER control group

Study Locations (1)

Alabama

  • UAB - Birmingham

Trial Details

FieldValue
Enrollment Target 190 participants
Start Date 2025-02-13
Est. Completion 2030-11-30
Phase Phase 1

Sponsor

University of Alabama at Birmingham

1,160 total trials

What the Registry Record Tells You About NCT06593093

The ClinicalTrials.gov registry entry for NCT06593093 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 190 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,656-participant average among 257 other Opioid Use Disorder trials with a reported enrollment target (96% lower). The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Opioid Use Disorder appearing as the primary indexed condition, and to 2 interventions - of which a bundled intervention is the first listed.

NCT06593093 reports 1 study location spanning 1 distinct geographic area - top geographies include Alabama.

Frequently Asked Questions

What is clinical trial NCT06593093 about?

NCT06593093 is a clinical study titled "A Bundled Intervention". Opioid overdose deaths have reached historically high records in the United States and are particularly concentrated among patients after emergency department (ED) discharge. Evidence-based treatment modules to reduce repeat opioid overdose and mortality are lacking in this patient population. A bun...

What is the current status of trial NCT06593093?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 190 participants. The study started on 2025-02-13. Estimated completion is 2030-11-30.

What conditions does trial NCT06593093 study?

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

What interventions are being tested in trial NCT06593093?

The interventions under investigation include: a bundled intervention (OTHER), control group (OTHER).

Who is sponsoring clinical trial NCT06593093?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06593093 being conducted?

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

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