This research protocol will compare Theramine to a non-steroidal anti-inflammatory drug (NSAID) in the treatment of chronic back pain. The study will examine the efficacy and tolerability of Theramine alone in patients with chronic back pain in comparison to the NSAID, Naproxen, and the co-administration of Naproxen with Theramine.
After informed consent and screening, volunteers will be entered into a double blind, randomized, three-armed trial, with 40 patients in each group. Patients will receive either Naproxen 250 mg daily, Theramine 2 capsules two times daily, or the co-administration of low-dose Naproxen 250 mg daily with Theramine 2 capsules two times daily for 28 days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
127
Co-administration of Theramine and Naproxen, CoPack Kit Theraproxen
Theramine, a medical food, co-administered with naproxen-like placebo
naproxen co-administered with Theramine-like placebo.
Roland-Morris Lower Back Pain Scale
The primary efficacy outcome will be the change from baseline in awakening stiffness and pain subscale scores obtained from the Roland-Morris Lower Back Pain Scale.
Time frame: Baseline and Day 28
Oswestry Low Back Pain Scale
Change measured in Oswestry low back pain scale.
Time frame: Baseline and Day 28
Visual Analog Scale
Change measured in visual analog scale.
Time frame: Baseline and Day 28
Blood Panel
Baseline and day 28 blood measurement, CBC, liver panel, CRP.
Time frame: Baseline and Day 28
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.