OpalGenix- Personalized Postoperative Pain Management Following Lumbar Spinal Fusion and Decompression Surgery in Adults

Recruiting Observational Study
Lumbar Spine Stenosis Lumbar Spine Degeneration
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 99
Sex
Any
Study type
Observational
Participants needed
235 (estimated)
Sponsor
OpalGenix, Inc · Industry
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About This Trial
The proposed research is an important extension of an ongoing perioperative personalized analgesia and intravenous opioid pharmacogenetic research. This research focuses on two of the most commonly used oral opioid analgesics, oxycodone, and methadone, in adults following lumbar spinal fusion and decompression surgery. Genetic signature and combinatorial pharmacogenetic approaches perform better t…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * \>18 years of age * American Society of Anesthesiologists (ASA) Physical Status 1, 2, or 3 * Undergoing lumbar spine surgeries (lumbar spine decompression, multilevel posterior spine fusion, internal fixation or a combination) for degenerative lumbar spine and lumbar spinal st…
Contacts

Amy Monroe, MPH, MBA

412-623-6382

monroeal@upmc.edu

CONTACT

Alisha Maslanka, BS

412-864-6779

maslankaa@upmc.edu

CONTACT