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NCT03489161 · ClinicalTrials.gov registry record · Early Phase 1

Feasibility of the Utilization of Buprenorphine in the Emergency Room to Treat Clinical Opioid Withdrawal

A Early Phase 1 study, sponsored by Virginia Commonwealth University.

Completed
Registry status
Early Phase 1
Development phase
3
Enrollment target

NCT03489161: Completed Early Phase 1 study, sponsored by Virginia Commonwealth University.

NCT03489161 is a Early Phase 1 study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 3 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03489161, a Early Phase 1 study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
Early Phase 1
Development phase
3 participants
Enrollment target

Study Summary

The investigators are trying to determine whether they can effectively treat patients suffering from acute opioid withdrawal in the Emergency Department at Virginia Commonwealth University Health System (VCUHS) and subsequently transfer them to an outpatient addiction clinic within the existing infrastructure. This will be a descriptive investigation of the process to reveal areas of success and opportunities for improvement in order to determine feasibility of the study procedures in preparation for a larger clinical investigation.

Primary Outcome

Percentage of eligible potential participants who enroll in study

Interventions

  • DRUG Buprenorphine

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2018-08-01
Est. Completion 2018-08-28
Phase Early Phase 1
Virginia Commonwealth University

558 total trials

What the finished NCT03489161 record still lists

NCT03489161 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (94% lower).

The record links to 0 conditions, and to 1 intervention - of which Buprenorphine is the first listed.

NCT03489161 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03489161 about?

NCT03489161 is a clinical study titled "Feasibility of the Utilization of Buprenorphine in the Emergency Room to Treat Clinical Opioid Withdrawal". The investigators are trying to determine whether they can effectively treat patients suffering from acute opioid withdrawal in the Emergency Department at Virginia Commonwealth University Health System (VCUHS) and subsequently transfer them to an outpatient addiction clinic within the existing infr...

What is the current status of trial NCT03489161?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 3 participants. The study started on 2018-08-01. Estimated completion is 2018-08-28.

What interventions are being tested in trial NCT03489161?

The interventions under investigation include: Buprenorphine (DRUG).

Who is sponsoring clinical trial NCT03489161?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03489161's enrollment target sits among peer trials

3 1949th of 2000 higher than 28 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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 NCT03489161, the US trial registry maintained by the National Library of Medicine. NCT03489161 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.