What this study is
This research study will evaluate the use of, and participants experience with, a new device called Addinex that safely stores and dispenses opioid medication. The purpose of this study is to evaluate the use of the Addinex device in cancer patients undergoing cancer-related surgery that require pain control with opioids after the surgery. Participants will be asked to answer questions about their medical history and background, fill out questionnaires, use a mobile application associated with the device, and undergo a phone interview one month after stopping use of the device. This study aims to find out how participants like using the Addinex device as opposed to a traditional pill bottle. Results of this study will help determine if the Addinex device could be useful to patients in the future after surgeries, as opposed to typical pill bottles.
What's being tested
- Addinex Device (ADX-27)
Intervention · DEVICE
The device operates without the use of any electronics, wireless or firmware requirements. This is achieved through its mechanical system which uses a different randomized "passcode" for each dose that is loaded into a circular drum inside the device. The "passcodes" are provided by an online server through either a mobile app, web app, text service or call in service. The online server provides "passcodes" on a request basis, while following instructions set by the treating physicians.
Study details
- Official title
- Efficacy of a Pill-Dispensing System to Increase Disposal of Unused Opioids and to Reduce Refills After Cancer-Related Surgery
- Sponsor
- Columbia University
- Conditions
- Opioid Use · Breast Cancer
- Enrolling
- 140 people
- Starts
- 2020-10-05
- Est. completion
- 2027-07
- Design
- Open-label, single group
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 99 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Adult patients (age greater than or equal to 18 years)
- Planned for major cancer-related surgery and expected to receive a postoperative opioid prescription
- Must speak English or Spanish
- Must have access to a smartphone or an alternative smart device (e.g., iPhone, Android phone, iPad, Surface, etc.).
- Co-enrollment in trials involving pharmacologic therapy is allowed
You can't join if
- Patients who are taking opioids daily prior to the surgical procedure
- Patients unable to physically utilize the device
- Patients unable to self-administer medications
- Patients uncomfortable with using iPhone or iPad-based technology
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (1)
1 openColumbia University Medical Center
New York, New York, United States
- Dawn Hershman, MD · Contact212-305-1945dlh23@cumc.columbia.edu
Recruiting
Study team
Sponsor
Columbia University
Study ID AAAS8214
Principal investigator
Dawn Hershman, MD
Columbia University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.