Addinex: Medication dispensing system to control and monitor opioid use
Standard Pill Bottle: Access and use of opioids in a standard pill bottle.
Study summary
The goal of this study is to analyze the use of the Addinex system for opioid dispensing after ambulatory care to determine whether it will reduce opioid consumption, increase pill disposal, show variables that may predict opioid consumption, and determine whether this intervention is acceptable to patients.
Eligibility
Sex
ALL
Min age
6 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Ages six years and older
* Ability to swallow pills
* Isolated bone fracture
* Planned to receive opioids in the post-treatment period
* Not taking opioids daily prior to the procedure
* English or Spanish-speaking
* Able to give informed consent or a parent that can give informed consent
* Ownership of and comfort using apps on a smartphone with compatible operating system
* WIFI or cellular access
* Patient not admitted to hospital
Exclusion Criteria:
* Recent opioid use (last 30 days or 2 or more prescriptions in the past 3 months
* Impaired decisional capacity
* In police custody
* Ward of the state
Primary outcome measure(s)
Median pill consumption — One month post treatment Patients are expected to consume at least 16% fewer pills/MMEs using the Addinex system as compared to the control group.
Trial sites (1)
Facility
City
Region
Status
Rhode Island Hospital/Lifespan
Providence
Rhode Island
Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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