Actively Recruiting
Opioid Dispensing Device for Post-Operative Pain in Cancer Patients
Led by Columbia University · Updated on 2025-05-31
140
Participants Needed
1
Research Sites
290 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Opioid Dispensing Device for Post-Operative Pain in Cancer Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients age 18 years or older
- Planned for major cancer-related surgery with expected postoperative opioid prescription
- Able to speak English or Spanish
- Have access to a smartphone or a smart device such as iPhone, Android phone, iPad, or Surface
- Co-enrollment in trials involving pharmacologic therapy is allowed
You will not qualify if you...
- Taking opioids daily before the surgery
- Unable to physically use the Addinex device
- Unable to self-administer medications
- Uncomfortable using iPhone or iPad-based technology
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Columbia University Medical Center
New York, New York, United States, 10032
Actively Recruiting
Research Team
R
Research Nurse Navigator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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