User Acceptability of a Device-Based Opioid Overdose Intervention

Completed

Conditions studied: Opioid Overdose, Opioid-use Disorder, Substance Use Disorders

In brief

This pilot study evaluates the needs of opioid users for a device-based intervention for opioid overdoses. The results of this one-time short questionnaire will inform development of a novel naloxone delivery device.

Key facts

Study ID

NCT04530591

Run by

University of Pennsylvania

People needed

97

Starts

2020-08-25

Expected to finish

2020-09-15

Last updated by the study team

2021-07-07

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have used opioids for more than 3 months or will be having surgery where opioids will be administered
• Able to provide informed consent
• Moderate to severe chronic pain treated with opioids or recreational use

You may not qualify if…

• Pregnancy

Where it is running

• Prevention Point Philadelphia — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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