Effect of Artronat on the Quality of Life of Patient With Osteoarthritis

Lescuyer Laboratory

Status: Completed

Conditions: Osteoarthritis

Treatments: Dietary Supplement: PLACEBO; Dietary Supplement: ARTRONAT

Study type: Interventional

Funder types: Industry; Other

Identifiers

NCT01356199

2011-A00319-32

Details and patient eligibility

About

The purpose of this study is to determine whether the nutritional supplement ARTRONAT improves the quality of life of patients with osteoarthritis.

Full description

Osteoarthritis is a degenerative disease that greatly impairs the quality of life of patients. A nutritional supplement may help, in association with the normal treatment of osteoarthritis, improving the quality of life of such patients, in reducing pain and/or improving join flexibility.

Enrollment: 7 patients

Sex: All

Ages: 40 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• age 40-75 years
• BMI 18.5-30
• osteoarthritis type II or III

Exclusion criteria

• osteoarthritis type I or IV
• allergy to one of the component of the supplement
• blood pressure > 14/8
• history of knee surgery

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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7 participants in 2 patient groups, including a placebo group

ARTRONAT

Experimental group

Treatment:

Dietary Supplement: ARTRONAT

PLACEBO

Placebo Comparator group

Treatment:

Dietary Supplement: PLACEBO