Observational Study Linking Genetic Variants With Clinical Outcomes in Pain Management
Status unconfirmed
Conditions studied: Pain, Chronic Pain
In brief
The purpose of this study is to (a) evaluate the treatment approaches and changes in treatment regimens utilized by clinicians when genetic testing is performed in the clinic; and (b) create a patient data registry to identify genetic factors that influence treatment outcomes in pain management.
Key facts
- Study ID
- NCT02480075
- Run by
- Proove Bioscience, Inc.
- People needed
- 2000
- Starts
- 2015-11-01
- Expected to finish
- 2020-08-01
- Last updated by the study team
- 2016-03-30
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Provide signed and dated informed consent form.
- Willing to comply with all study procedures and be available for the duration of the study.
- Currently experiencing a chronic pain problem, with symptoms that have occurred within the last 30 days.
You may not qualify if…
- Severe hepatic or renal disease
- Significant diminished mental capacity that is unable to understand the protocol, surveys and questionnaires; unable to read/write English or Spanish
- Recent febrile illness that precludes or delays participation by more than 1 month
- Pregnancy or lactation
- Participation in a clinical study that may interfere with participation in this study
- Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study
Where it is running
- Pain Clinic at University of Southern California Keck Medical Center — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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