Chronic Low Back Pain Clinical Trial
Official title:
A Double Blind Placebo Study to Determine the Effectiveness of Theramine on the Management of Chronic Back Pain
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, Ibuprofen, and the co-administration of Ibuprofen with Theramine.
The diagnosis and management of back pain is a challenge for both primary care physicians
and specialists. Establishing an etiology can be difficult and often problematic, with
treatment options capable of producing serious and potentially life threatening side
effects. Treatments often exert a modest impact on the natural history of the condition.
Non-steroidal anti-inflammatory drugs (NSAIDs) are frequently prescribed to treat chronic
back pain. NSAIDs are only moderately effective in relieving pain. NSAIDs are the leading
cause of drug-induced gastrointestinal bleeds, the most common cause of drug-induced
morbidity and mortality particularly at high dose. They can also exacerbate hypertension,
edema and produce nephrotoxicity. The effects are also dose dependent. Recent data indicates
NSAIDs are a risk factor for myocardial infarction, particularly at high doses. Recent data
also indicates NSAIDs disrupt collagen repair in injured tissue. Muscle relaxants and
narcotic analgesics show limited efficacy and often produce sedation, constipation or
inappropriate usage. Physical therapy and local modalities often are not satisfying, costly,
and require considerable investment of patient time.
Neurotransmitter depletion has been demonstrated to contribute to chronic pain states.
Increased nutrient requirements associated with pain syndromes and the consequent reduced
production of neurotransmitters contribute to maladaptive pain responses. The ability to
enhance neurotransmitter production associated with pain syndromes is limited by multiple
factors, specifically unavailability of adequate essential amino acids in the diet and
increased turnover rates of amino acids needed to produce neurotransmitters in pain
syndromes. Other factors such as prolonged pharmaceutical use deplete the nerve cells of
neurotransmitters. Attempts to modify brain neurochemistry have focused on single
neurotransmitters such as serotonin or GABA. However, this approach fails to address the
complexity and complementary influences of multiple neurotransmitters on patient perception
of pain and suffering.
Theramine is a proprietary prescription Medical Food which concurrently enhances several
neurotransmitters that are involved in pain modulation and sensation by providing
neurotransmitter precursors in the form of amino acids, (see attached Monograph for detailed
discussion). Small trials have found Theramine effective in reducing and modifying pain
without demonstrable side effects. Theramine simultaneously stimulates the production of the
neurotransmitters serotonin, GABA, brain induced cortisol, nitric oxide, and glutamate.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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