Collecting Outcomes and Managing Pain After Surgery

Recruiting N/A Interventional Study
Surgery
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 90
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
10,000 (estimated)
Sponsor
Duke University · Other
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About This Trial

The primary aim of this study is to measure pain and psychosocial patient reported outcomes, objective functionality, and actual daily at home opioid usage in orthopedic patients. The study's goal following the data collection is to predict which patients are at high risk for chronic opioid use.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * aged 18-90 years old who are undergoing elective orthopedic surgery at Duke Health. * Patients must have their own smartphone IOS or Android device. * Patients must be able to read English. Exclusion Criteria: * Lacking capacity to provide consent. * Cannot read English * Un…
Contacts

Ashley Burke

+1 919 681 2849

ashley.burke@duke.edu

CONTACT

Michael Bullock, MD

+1 919 668 2024

william.bullock@duke.edu

CONTACT