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Chronic Low Back PainPhase 4NCT01490905

A Double Blind Placebo Study to Determine the Effectiveness of Theramine on the Management of Chronic Back Pain

A Phase 4 study testing Theramine (A medical food), Theraprofen and Ibuprofen in people with Chronic Low Back Pain, run by Targeted Medical Pharma at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Chronic Low Back Pain
What is being tested?
Theramine (A medical food), Theraprofen and Ibuprofen
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
127 participants
Where
1 siteUnited States
Study dates
Sep 2010to Apr 2011
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Back pain lasting greater than six (6) weeks. Pain must be present on at least 5 out of 7 days during each of the two weeks prior to screening visit
  • Analgesic medication used to treat pain at least 4 out of last 7 days and at least 10 days in the last month
  • Men and non-pregnant, non-lactating women over the age of 18 and under the age of 75, able to read, understand and sign English-language informed consent, with diagnosis of back pain and baseline back pain greater than 40 mm out of 100 mm on visual analog scale
  • Those taking an NSAID for pain must discontinue use during a washout period based on the attached five (5) half-lives of drug chart
  • If undergoing physical therapy for back pain, therapy must be stable at least three (3) weeks prior to study and remain the same throughout study
  • If using psychoactive medication which might have analgesic effects, (i.e. anti-depressants or anti-convulsants-), treatment must be stable for at least three (3) months prior to study
  • For men and women of child-bearing potential, must be willing to use adequate contraception and not be pregnant or impregnate their partner during the entire time of study
  • Must be willing to commit to all clinical visits during study-related procedures, including required discontinuation (washout) of analgesic or anti-inflammatory medication prior to Day 1 randomization. The patient must agree to using acetaminophen for rescue medication

Who cannot join

  • Patients with back surgery in the past six (6) months
  • Patients with significant neurologic impairment, as diagnosed on screening physical examination
  • Patients with evidence or history of fracture of the spine in the past year
  • Patients not fluent in English
  • Use of aspirin for non-arthritic conditions, unless at a dose less than or equal to 325 mg a day, and must be stable for at least one (1) month prior to screening
  • Use of controlled substances and/or opiate analgesic for pain, for more than 5 days within the last 30 days prior to screening visit
Show all 12Show fewer
  • Receipt of an oral intramuscular or soft-tissue injection of corticosteroid within one (1) month prior to screening
  • Participation in a clinical trial within the one (1) month prior to screening
  • History of epidurals in the past three (3) months
  • History of alcohol or substance abuse
  • Uncontrolled or unstable serious cardiovascular, pulmonary, gastrointestinal or urogenital, endocrine, neurologic or psychiatric disorder
  • History of gastrointestinal bleed or documented gastric or duodenal ulcer

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Targeted Medical Pharma

    Los Angeles, California, 90077

Other trials in United States

About this study

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.

Read the detailed description

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.

Being tested
Theramine (A medical food), Theraprofen, Ibuprofen
Keywords
Medical food, Theramine, Ibuprofen, Amino acids, Convenience Pack Kit

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Theramine (A medical food)Other

    Theramine two capsules twice daily for 28 days.

  • TheraprofenDrug

    Theramine two capsules twice daily and ibuprofen 400mg once daily for 28 days.

  • IbuprofenDrug

    Ibuprofen 400mg once daily for 28 days.

Study groups in NCT01490905
Study groupRoleWhat they receive
Theramine active and ibuprofen placeboActive comparator2 capsules Theramine twice daily with one ibuprofen-like placebo once daily.
Receives: Other: Theramine (A medical food)
Theramine and Ibuprofen (Theraprofen)Active comparatorTwo capsules Theramine twice daily with Ibuprofen 400mg once daily.
Receives: Drug: Theraprofen
Theramine placebo and IbuprofenActive comparatorTwo Theramine-like placebo twice daily and one ibuprofen 400mg.
Receives: Drug: Ibuprofen

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: 28 Days

Secondary outcomes (5)
  1. Visual Analog Scale Evaluation

    The primary efficacy outcome will be the change from baseline in awakening stiffness and pain subscale scores obtained from the Visual Analog Scale Evaluation.

    Measured: 28 days

  2. Oswestry Low Back Pain Scale

    Functionality outcomes obtained from the Oswestry Low Back Pain Scale

    Measured: 28 Days

  3. C-reactive protein

    Percent change in c-reactive protein levels from baseline to Day 28.

    Measured: 28 Days

  4. Interleukin-6

    Percent change in Il-6 level from baseline to Day 28.

    Measured: 28 Days

  5. Amino Acid Panel

    Change in amino acid turnover rate from baseline to Day 28.

    Measured: 28 Days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Dec 2011 (estimated)
  2. Study startSep 2010
  3. Primary completionFeb 2011
  4. Study completionApr 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
127 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01490905
Sponsor's protocol ID
0820102
Status last verified
Dec 2011
First submitted
22 Nov 2011
Last updated
13 Dec 2011
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Theramine (A medical food), Theraprofen and Ibuprofen in people with Chronic Low Back Pain, run by Targeted Medical Pharma at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Dec 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Roland-Morris Lower Back Pain Scale (time frame: 28 Days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Dec 2011.

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