Clinical Study to Evaluate Clinical Impact of PGx-Guided Treatment for Patients Undergoing Elective Spinal Surgical Procedures
Acute Pain, Surgery
About this trial
This is an interventional diagnostic trial for Acute Pain focused on measuring PGx, pharmacogenetic testing, IDgenetix, Pain Management, AltheaDx, Post-Operative Pain Management
Eligibility Criteria
Inclusion Criteria:
- Male or female subjects over the age of 18;
- Patients undergoing an elective spine surgical procedures
- Willing and able to comply with study procedures
- Able to provide written informed consent
- Surgery timing - scheduled to occur after PGx testing and IDgenetix test report review (at least 4 days after Pre-Op visit)
Exclusion Criteria:
- Unwilling or unable to provide written informed consent and to comply with study procedures
- Any subject for whom providing a buccal swab sample would be contraindicated or not possible
- Subject with a history of chronic renal dysfunction, Chronic Kidney Disease (Stage 4 or 5)
- abnormal hepatic function within the last 2 years (INR >1.2 not attributable to anticoagulant medications, AST/aspartate aminotransferase or ALT/alanine aminotransferase >1.5x normal, or suspected cirrhosis)
- a history of malabsorption (short gut syndrome)
- any gastric or small bowel surgery less than 3 months prior to study enrollment
- Patients with a significant unstable medical condition or life threatening disease
- History of prior pharmacogenetic testing
Sites / Locations
- Ochsner Health System
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
NeuroIDgenetix Test Panel Intervention
Control
The medical provider for the NeuroIDgenetix-guided group will make post-operative pain management recommendations based on test results. Patient outcomes, length of hospital stay and number of medical visits will be measured throughout the study.
The medical provider for the control group will not receive the NeuroIDgenetix Test Panel results and will make post-operative pain management recommendations based as usual. Patient outcomes, length of hospital stay and number of medical visits will be measured throughout the study.