Quell Opioid Reduction and Pain Relief in Patients With Cancer
Stopped early · Not applicable · Has a placebo group
Conditions studied: Pain, Metastatic Breast Cancer, Prostate Cancer, Colorectal Cancer
In brief
To study effects the Quell device has on opioid consumption and pain relief in patients with cancer.
Key facts
- Study ID
- NCT02809846
- Run by
- Scripps Translational Science Institute
- People needed
- 33
- Starts
- 2016-07-01
- Expected to finish
- 2017-10-01
- Last updated by the study team
- 2020-01-21
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or Female greater than or equal to 18 year of age at visit one.
- Documented diagnosis of metastatic breast, prostate or colorectal cancer with a prognosis of 6 month or greater as determined by the primary oncologist.
- Visual evidence that subject owns a smart phone and is able to use basic mobile applications such as downloading an app, opening the app, and performing one simple task within the app.
- Subject speaks and reads English fluently.
- Subject able to understand and grant informed consent.
- Live in an area with cellular data connectivity available as provided by the subject.
- Documented adherence with clinic follow up visits per medical records.
- Subject using at least one opioid medication on a daily basis.
You may not qualify if…
- Subject has a cardiac pacemaker, implanted defibrillator or other implanted electronic device.
- Inability to complete subjective data as required; e.g. on mobile application and questionnaires.
- Does not live in an area with suitable cellular data connectivity.
- Has infrequent scheduled clinic visits.
Where it is running
- Scripps Translational Science Institute — La Jolla, California, United States
Full record on ClinicalTrials.gov
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