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N/A N=395 Prevention

Naloxone Auto-injector as a Universal Precaution for Patients With Opioid Use Disorder

Opiate Antagonist Overdose · Opioid-Related Disorders

Enrolled (actual)
395
Serious AEs
0.0%
Results posted
Aug 2024
Primary outcome: Primary: To Measure the Association of Take-home Naloxone With Overdose Reversals Performed by Patients With Opioid Use Disorder Enrolled in an Opioid Treatment Program — 73; 263 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Naloxone Auto-Injector (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of New Mexico
Primary completion
May 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
To Measure the Association of Take-home Naloxone With Overdose Reversals Performed by Patients With Opioid Use Disorder Enrolled in an Opioid Treatment Program
73; 263

Summary

The purpose of this pilot-study is to to distribute naloxone auto-injector in a "Universal Precaution" manner to patients with opioid substance use disorder. The objectives are to decrease the number of fatal and nonfatal overdose deaths, to examine and understand the risk factors for serious opioid toxicity and overdose, and to evaluate the unintentional opioid overdose risk utilizing an evidence-based screening questionnaire.

Eligibility Criteria

Inclusion Criteria

  • All patients treated with methadone, naltrexone or buprenorphine as medication assisted treatment at the UNM Addiction and Substance Abuse Program (UNM ASAP) aged 18 or older

Exclusion Criteria

  • Subjects who are allergic to naloxone and its inactive ingredients. Inactive ingredients include buffering agents.
  • Subjects younger than 18.
  • Subjects not being treated at UNM ASAP.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02669901). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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