Clinical Trials Directory

Trials / Completed

CompletedNCT01527994

Aprepitant Effects in Intravenous Heroin Dependence

Clinical Laboratory Evaluations of Aprepitant for the Treatment of Opioid Dependence: Inpatient Test

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
64 (actual)
Sponsor
NYU Langone Health · Academic / Other
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

Current treatments for opioid addiction would benefit by the addition of a non-opioid based treatment medication. Recent behavioral studies have shown that the neurokinin-1 (NK1) receptor is involved in opioid reward and withdrawal. This study proposes to study a potential non-opioid treatment, the clinically available, FDA approved, NK1 antagonist aprepitant, in opioid addicted patients. Based on the unique behavioral and pharmacological characteristics of opioid addiction, and what is known of the currently employed treatments, the investigators propose that the therapeutic mechanism of any potential opioid addiction treatment medication must include the ability to reduce opioid withdrawal. This is of particular importance during treatment initiation (eg. detoxification). In addition, for long-term treatment and relapse prevention, it is important to manage drug craving and inhibit the rewarding effects of opioids if patients do experience a slip. Therefore, the investigators propose to study aprepitant using human models of opioid withdrawal, craving and acute opioid reward and reinforcement. The investigators will also include a neuro-economics choice procedure paradigm.

Conditions

Interventions

TypeNameDescription
DRUGAprepitantAprepitant 125 mg oral tablets
DRUGPlacebo pillPlacebo oral pill- inactive compound

Timeline

Start date
2012-01-01
Primary completion
2014-06-01
Completion
2015-02-01
First posted
2012-02-07
Last updated
2021-08-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01527994. Inclusion in this directory is not an endorsement.