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Clinical Trial
. 2015 Dec;23(12):2102-2108.
doi: 10.1016/j.joca.2015.06.007. Epub 2015 Jun 20.

Huo-Luo-Xiao-Ling (HLXL)-Dan, a Traditional Chinese Medicine, for patients with osteoarthritis of the knee: a multi-site, randomized, double-blind, placebo-controlled phase II clinical trial

Affiliations
Clinical Trial

Huo-Luo-Xiao-Ling (HLXL)-Dan, a Traditional Chinese Medicine, for patients with osteoarthritis of the knee: a multi-site, randomized, double-blind, placebo-controlled phase II clinical trial

L Lao et al. Osteoarthritis Cartilage. 2015 Dec.

Abstract

Objective: To examine the efficacy and safety of Huo-Luo-Xiao-Ling (HLXL)-Dan, a Traditional Chinese Medicine (TCM), in patients with knee osteoarthritis (OA).

Design: A multi-site, randomized, double-blind, placebo-controlled phase II dose-escalation clinical trial was conducted. Eligible patients who fulfilled American College of Rheumatology criteria were randomized to receive either HLXL or placebo. Clinical assessments included measurement of knee pain and function with the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), patient global assessment (PGA), and knee pain scores every 2 weeks. A Data and Safety Monitoring Board (DSMB) was established to review the data for ensuring the quality of the trial.

Results: In the first stage, 28 participants were randomized to receive either low-dose HLXL-Dan (2400 mg/day) or placebo for 6 weeks. The results showed no statistical difference between the two groups. The study was then re-designed following the recommendation of DSMB. Ninety-two patients were enrolled in the second stage and were randomized to receive either high-dose HLXL-Dan (4000 mg/day for week 1-2, and 5600 mg/day for week 3-8) or placebo for 8 weeks. All outcome assessments showed significant improvements for both groups after 8 weeks but no significant between-group differences. The change (mean ± SD) of WOMAC pain and WOMAC function scores of HLXL and placebo group after 8 weeks were -1.2 ± 1.7 vs -1.4 ± 1.5, and -1.1 ± 1.6 vs -1.3 ± 1.5 respectively. No serious adverse events were reported.

Conclusion: Although safe to use, an 8-week treatment of HLXL-Dan was not superior to placebo for reduction in pain or functional improvement in patients with knee OA.

Clinical trial registration number: Clinicaltrials.gov (NCT00755326).

Keywords: Chinese herbs; Huo-Luo-Xiao-Ling-Dan; Knee osteoarthritis; Randomized controlled trial; Traditional Chinese medicine.

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Conflict of interest statement

Competing interest statement

All authors declared no conflicts of interest.

Figures

Figure 1
Figure 1
HPLC chromatogram of HLXLa, b a (1) = Boswellia carterii, (2) =Notopterygium incisum, (3) = Angelica sinensis, (4) = Paeonia lactiflora, (5) = Glycyrrhiza uralensis (6) =Corydalis yanhusuo, (7) = Salvia miltiorrhiza (8) = Ligusticum chuanxiong, (9) = Gentiana macrophylla, (10) = Cinnamomum cassia, (11) = Angelica pubescens. b(1)-1, (1)-2, (1)-3 = Boswellia carterii characteristic peaks 1, 2 and 3 respectively; (2)-1, (2)-2, (2)-3, (2)-4 = Notopterygium incisum characteristic peaks 1, 2, 3 and 4 respectively; etc.
Figure 2
Figure 2
Patient Flowchart (High-Dose Trial)

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