Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00158184 · ClinicalTrials.gov registry record · Phase 2

Prescription Opioid Effects in Abusers Versus Non-Abusers

A Phase 2 study, sponsored by New York State Psychiatric Institute.

Completed
Registry status
Phase 2
Development phase
27
Enrollment target

NCT00158184: Completed Phase 2 study, sponsored by New York State Psychiatric Institute.

NCT00158184 is a Phase 2 study that has completed, run by New York State Psychiatric Institute. The registered enrollment target is 27 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00158184, a Phase 2 study, has completed, sponsored by New York State Psychiatric Institute.

COMPLETED
Registry status
Phase 2
Development phase
27 participants
Enrollment target

Study Summary

The purpose of this study is to examine the abuse liability of oxycodone in individuals with, and without, a history of prescription opioid abuse.

Primary Outcome

Maximum number of finger presses on a computer mouse completed. The "Breakpoint" is the amount of work (clicks on a mouse) participants were willing to do in order to received the dose of drug under investigation. This is a commonly used indicator of a drugs value and abuse liability.

Interventions

  • DRUG oxycodone 15 mg
  • DRUG oxycodone 30 mg
  • DRUG Placebo 0 mg

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2004-06
Est. Completion 2009-06
Phase Phase 2

What the finished NCT00158184 record still lists

NCT00158184 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 3 interventions - of which oxycodone 15 mg is the first listed.

NCT00158184 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00158184 about?

NCT00158184 is a clinical study titled "Prescription Opioid Effects in Abusers Versus Non-Abusers". The purpose of this study is to examine the abuse liability of oxycodone in individuals with, and without, a history of prescription opioid abuse.

What is the current status of trial NCT00158184?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 27 participants. The study started on 2004-06. Estimated completion is 2009-06.

What interventions are being tested in trial NCT00158184?

The interventions under investigation include: oxycodone 15 mg (DRUG), oxycodone 30 mg (DRUG), Placebo 0 mg (DRUG).

Who is sponsoring clinical trial NCT00158184?

This trial is sponsored by New York State Psychiatric Institute, which has 364 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00158184's enrollment target sits among peer trials

27 1697th of 2000 higher than 293 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00912041 · 27 participants · NA

    BrainGate2: Feasibility Study of an Intracortical Neural Interface System for Persons With Tetraplegia

  • NCT02847559 · 27 participants · Phase 2

    Optune Delivered Electric Field Therapy and Bevacizumab in Treating Patients With Recurrent or Progressive Grade 2 or 3 Meningioma

  • NCT03380195 · 27 participants · NA

    Effects of Watermelon Juice on Heart Rate Recovery and Post-exercise Muscle Soreness

  • NCT03384238 · 27 participants · Phase 1

    Panitumumab-IRDye800 in Patients With Pancreatic Cancer Undergoing Surgery

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00158184, the US trial registry maintained by the National Library of Medicine. NCT00158184 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.