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

Completed · Phase 4 · Has a placebo group

Conditions studied: Chronic Low Back Pain

In brief

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.

Key facts

Study ID

NCT01490905

Run by

Targeted Medical Pharma

People needed

127

Starts

2010-09-01

Expected to finish

2011-04-01

Last updated by the study team

2011-12-13

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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
• 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

Where it is running

• Targeted Medical Pharma — Los Angeles, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.