N/A
N=97
User Acceptability of a Device-Based Opioid Overdose Intervention
Opioid Overdose · Opioid-use Disorder · Substance Use Disorders
Bottom Line
View on ClinicalTrials.gov: NCT04530591 ↗Enrolled (actual)
97
Serious AEs
—
Results posted
Jul 2021
Primary outcome: Primary: Community Need for a Device-based Opioid Overdose Intervention — 69; 22 Participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Survey (Other); Interview (Other)
- Age
- Adult, Older Adult · 21+ yrs
- Sex
- All
- Sponsor
- University of Pennsylvania
- Primary completion
- Sep 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Community Need for a Device-based Opioid Overdose Intervention |
69; 22 | — |
| SECONDARY Functional and Aesthetic Preferences for Device-based Opioid Overdose Intervention |
70; 26; 66; 29; 52; 44 | — |
Summary
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.
Eligibility Criteria
Inclusion Criteria
- 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
Exclusion Criteria
- Pregnancy
Data sourced from ClinicalTrials.gov (NCT04530591). 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.