Pain Clinical Trial
Official title:
Investigation of Kritech Efficacy on Subjects Having Functional Discomfort Associated to Joints and Muscles Disorders
Joints and muscles disorders are common symptoms in the population. They are characterized by swelling, pain, functional impairment and morning stiffness. These disorders can be really disabling and painful, affecting the person's quality life. The purpose of this clinical trial is to test Kritech (Krill oil) efficacy in reducing these symptoms in 154 subjects complaining functional discomfort associated to joints and muscles disorders.
Epidemiological studies on prevalence and incidence of joints and muscles disorders are
scares. Two epidemiological French studies recorded patients consulting their GP for
widespread pain, whatever the cause. The most often cited pain localization was the
musculoskeletal system (36-59% of the cases). In Europe the situation is similar, with
arthritis and osteoarthritis representing the 42% of pains. According to the WHO (World
Health Organization) the musculoskeletal system's disorders are the first cause of handicap
in the worldwide population.
Krill oil is low in both saturated fatty acids and monounsaturated fatty acid and high in
polyunsaturated fatty acid including a high proportion of (n-3) fatty acids and particularly
EPA and DHA. There are strong evidences that krill oil may improve the comfort of sensitive
joints thank to its n-3 fatty acids and phospholipids content. Particularly, after a
supplementation with a dietary product containing pure krill oil, a reduction of systemic
inflammation, trough reduction of CRP, was concomitantly accompanied by improvement of
various clinical scores associated with joint flexibility, comfort and function. Despite
this, there are no studies yet on healthy volunteers complaining the symptoms of
rheumatologic pathologies, without being ill.
Here we performed a clinical trial on 154 subjects complaining functional discomfort
associated to joints and muscles disorders. The principal objective was to test Kritech
efficacy in reducing these symptoms.
Subjects were split in two groups, with one receiving Kritech and the second one the placebo
for 12 weeks.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Supportive Care
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