Randomized controlled trial Targeted patients who come to receive treatment for osteoarthritis that meets the research indications will be assigned to a random group by the box of 4 randomization method, with a sequence that is randomly generated by a computer. The groups are divided into two groups: Group 1: Patients who have taken 480 mg of hydrolyzed collagen and 20 mg of undenatured type II collagen Group 2: Control patients will take placebo Primary outcome : Pain level
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
68
Prince of Songkla University
Hat Yai, Changwat Songkhla, Thailand
Pain (VNRS)
Pain level (verbal numerical rating scale :VNRS) - 0 is no pain and 10 is the worst pain
Time frame: 12 weeks
Knee and Osteoarthritis Outcome Score (KOOS)
Knee and Osteoarthritis Outcome Score (KOOS) - 100 indicates the best possible results and 0 the worst outcome
Time frame: 12 weeks
Rescue medication
Amount of pain medication intake
Time frame: 12 weeks
Patient satisfaction
Patient satisfaction (verbal numerical rating scale :VNRS) - (0-10; 0=worst and 10=best)
Time frame: 12 weeks
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