A Multicenter, Randomized, Double-Blinded, Placebo-Controlled Clinical Trial to Evaluate the Efficacy and Safety of a Krill Oil, Astaxanthin, and Oral Hyaluronic Acid Complex on Joint Health in People with Mild Osteoarthritis

被引:11
|
作者
Hill, W. Stephen [1 ]
Dohnalek, Margaret H. [1 ]
Ha, Yejin [2 ]
Kim, Seok-Jung [3 ]
Jung, Jae-Chul [2 ]
Kang, Seung-Baik [4 ]
机构
[1] US Nutraceut Dba Valensa Int, Eustis, FL 32726 USA
[2] NOVAREX Co Ltd, 80 Osongsaengmyeong 14 Ro, Chueongju Si 28220, South Korea
[3] Catholic Univ Korea, Uijeongbu St Marys Hosp, Coll Med, Dept Orthoped Surg, Uijeongbu Si 11765, South Korea
[4] Seoul Natl Univ, Boramae Hosp, Dept Orthoped Surg, Coll Med, Seoul 07061, South Korea
关键词
FlexProMD((R)); osteoarthritis; inflammation; joint pain; krill oil; astaxanthin; hyaluronic acid; KNEE OSTEOARTHRITIS; INFLAMMATORY CYTOKINES; CHONDROITIN SULFATE; WESTERN-ONTARIO; PAIN; GLUCOSAMINE; VALIDATION; DISABILITY; EXTRACTION;
D O I
10.3390/nu15173769
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Osteoarthritis is a significant global health problem. Many patients seek more effective alternatives to nonsteroidal anti-inflammatory medicines or commercial supplements to manage joint pain and inflammation. FlexPro MD (R) (FP-MD) combines krill oil, astaxanthin, and lower molecular weight hyaluronic acid to support joint health. A 12-week, randomized, double-blind, placebo-controlled trial compared the efficacy and safety of FP-MD and placebo once daily in participants (n = 100) with mild osteoarthritis of the knee or hip joint. For the primary endpoint of joint pain score, per-protocol participants (n = 75) in the FP-MD group (n = 37) had a statistically significantly greater mean reduction from baseline in the Korean Visual Analog Scale (K-VAS) at week 12 compared with participants in the placebo group (n = 38) (20.8 +/- 16.16 mm vs. 10.6 +/- 17.58, p = 0.0105). The Korean Western Ontario and McMaster Universities Osteoarthritis Index (K-WOMAC) total score was also significantly improved in the FP-MD group at week 12 compared with placebo (-13.0 +/- 13.62 vs. -5.5 +/- 18.08, p = 0.0489), especially an improvement in pain score (-2.5 +/- 2.92 vs. -1.3 +/- 3.94, p = 0.02635). FP-MD group had greater improvement in joint function scoring by investigator assessment (p = 0.0127) and by group participants (p = 0.0070). A statistically significantly greater number of patients reported adverse events in the placebo group compared with the FP-MD group (16% vs. 4%, p = 0.0455), most commonly gastrointestinal disorders in both of the groups. These findings suggest that FP-MD is well tolerated and can be effectively used to address joint pain in patients diagnosed with mild osteoarthritis, the main symptom of this condition.
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页数:16
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