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

NCT01395784 · ClinicalTrials.gov registry record · Phase 2

Effects of Pioglitazone, a PPARgamma Receptor Agonist, on the Abuse Liability of Oxycodone

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

Completed
Registry status
Phase 2
Development phase
32
Enrollment target

NCT01395784: Completed Phase 2 study, sponsored by New York State Psychiatric Institute.

NCT01395784 is a Phase 2 study that has completed, run by New York State Psychiatric Institute. The registered enrollment target is 32 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (76% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01395784, a Phase 2 study, has completed, sponsored by New York State Psychiatric Institute.

COMPLETED
Registry status
Phase 2
Development phase
32 participants
Enrollment target

Study Summary

The ability of pioglitazone (PIO) to alter the effects of opioids in humans has not been characterized in a controlled laboratory setting. Accordingly, the proposed investigation seeks to examine the effects of PIO on oxycodone, one of the most commonly used and abused opioid drugs in the U.S. (Davis et al., 2003). More specifically, the primary aim of this investigation is to characterize the subjective effects of oxycodone under maintenance on various doses of PIO (0, 15, and 45 mg) in non-dependent, prescription opioid abusers. Secondary aims of the study are to examine the influence of PIO on the analgesic, cognitive, and physiological effects of oxycodone.

Primary Outcome

Visual analog scale ratings (0-100 mm scale, 0=Not at all, 100=Extremely)

Interventions

  • DRUG pioglitazone

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2010-08
Est. Completion 2014-04
Phase Phase 2

What the finished NCT01395784 record still lists

NCT01395784 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (76% lower).

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

NCT01395784 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01395784 about?

NCT01395784 is a clinical study titled "Effects of Pioglitazone, a PPARgamma Receptor Agonist, on the Abuse Liability of Oxycodone". The ability of pioglitazone (PIO) to alter the effects of opioids in humans has not been characterized in a controlled laboratory setting. Accordingly, the proposed investigation seeks to examine the effects of PIO on oxycodone, one of the most commonly used and abused opioid drugs in the U.S. (Davi...

What is the current status of trial NCT01395784?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 32 participants. The study started on 2010-08. Estimated completion is 2014-04.

What interventions are being tested in trial NCT01395784?

The interventions under investigation include: pioglitazone (DRUG).

Who is sponsoring clinical trial NCT01395784?

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 NCT01395784's enrollment target sits among peer trials

32 1563rd of 2000 higher than 423 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

  • NCT02445781 · 32 participants · Early Phase 1

    Differing Levels of Hypoglycemia

  • NCT02792270 · 32 participants · NA

    Caloric Restriction In Sarcoma Patients Treated With Pre-Operative RT

  • NCT03068910 · 32 participants · Early Phase 1

    Hyperandrogenemia and Altered Day-night LH Pulse Patterns

  • NCT03208868 · 32 participants · NA

    Leucine Enriched Essential Amino Acid Mixture to Reverse Muscle Loss in Cirrhosis

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 NCT01395784, the US trial registry maintained by the National Library of Medicine. NCT01395784 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.