- Original Article
- Open Access
Effectiveness of intra-articular injections of sodium hyaluronate-chondroitin sulfate in knee osteoarthritis: a multicenter prospective study
© The Author(s) 2015
Received: 16 September 2015
Accepted: 28 October 2015
Published: 14 November 2015
The Erratum to this article has been published in Journal of Orthopaedics and Traumatology 2016 17:390
Intra-articular injection of hyaluronic acid is a well-established therapy for the treatment of knee osteoarthritis. The aim of the study was to assess the effectiveness and safety of the use of Arthrum HCS® (40 mg hyaluronic acid and 40 mg chondroitin sulfate in 2 mL).
Materials and methods
This was an open, multicenter, prospective study. Men or women over 40 years of age with documented knee osteoarthritis and WOMAC subscore A (severity of pain) ≥25 were enrolled. They received three weekly intra-articular injections of sodium hyaluronate 2 % and chondroitin sulfate 2 % in combination. WOMAC subscore A was assessed at 1, 3 and 6 months after the last injection.
One hundred and twelve patients were included (women, 66 %). The mean (SD) WOMAC subscore A decreased from 52.1 (15.2) at inclusion to 20.5 (19.7) at month 6 (P < 0.0001). The mean subscore was already significantly decreased 1 month after the last injection at 25.7 (P < 0.0001). Pain relief and consumption of analgesic drugs, both assessed with visual analogic scale (VAS), consistently decreased. The investigators were satisfied/very satisfied as regards the therapeutic effectiveness of sodium hyaluronate-chondroitin sulfate in reducing pain (77 %), improving mobility (78 %) and reducing the consumption of analgesics (74 %). Only one adverse effect was reported by one patient (knee tumefaction).
These results suggest that intra-articular injections of Arthrum HCS® (sodium hyaluronate plus chondroitin sulfate) in patients with knee osteoarthritis are efficient and safe. These results should be confirmed in a randomized controlled study.
Level of evidence
It is estimated that around 250 million people in the world are affected by knee osteoarthritis . Knee pain has an important impact by limiting activity and impairing quality of life. Thus, knee osteoarthritis has been identified as one of the medical conditions (with stroke, depression, hip fracture and heart disease) accounting for more physical disability than other diseases in people 65 years of age or older . Moreover, knee osteoarthritis has a major impact on healthcare costs [3–6].
The management of osteoarthritis should be hierarchical, with non pharmacological methods as first interventions (weight loss, exercise and braces), followed by analgesic drugs [nonsteroidal anti-inflammatory drugs (NSAIDs) and other analgesics], local therapies (topical NSAIDs, intra-articular corticosteroids and hyaluronic acid), and surgery as a last resort [7–10].
Administration of exogenous hyaluronic acid (viscosupplementation) directly into the joint is available as a treatment for the symptoms of knee osteoarthritis. The purpose of viscosupplementation is to overcome the qualitative and quantitative deficiency of hyaluronic acid that is associated with osteoarthritis. Hyaluronic acid is a polysaccharide that is the main constituent of cartilage and synovial fluid; it is responsible for the mechanical properties of the joint by allowing shock absorption, lubrication and cartilage protection . In osteoarthritis patients, synovial hyaluronate is depolymerized and is cleared at higher rates compared to normal subjects due to inflammation . Intra-articular injections of hyaluronic acid have been shown to be as effective as NSAIDs with fewer systemic adverse events ; this therapy has a delayed onset of action in comparison with intra-articular corticosteroids, but a longer-lasting benefit . Younger patients and patients at an earlier stage of the disease are more likely to benefit from viscosupplementation .
Arthrum HCS® (LCA Pharmaceutical, Chartres, France) is a new specialty for viscosupplementation combining sodium hyaluronate and chondroitin sulfate. Chondroitin sulfate—a sulfated glycosaminoglycan—is an important structural component of the extracellular cartilage matrix.
On the articular system, chondroitin sulfate links to monomers with high molecular weights. The proteoglycan aggregate exhibits viscoelastic and hydration properties and an ability to interact with the surrounding tissue through electric charges, leading to protection of the cartilaginous tissues. Furthermore, chondroitin sulfates are inhibitors of extracellular proteases involved in the metabolism of connective tissues and stimulate proteoglycan production by chondrocytes in vitro; they also inhibit cartilage cytokine production and induce apoptosis of articular chondrocytes . Preliminary clinical trials were in favor of the effectiveness of intra-articular injections of sodium hyaluronate-chondroitin sulfate. Thus, in a 3-month multicentric pilot study, a series of three weekly injections of a combination of hyaluronic acid-chondroitin sulfate was well tolerated and decreased pain in patients with knee osteoarthritis . A recent clinical study suggested that a single injection of sodium hyaluronate-chondroitin sulfate in patients with lateral epicondylitis offer better pain benefits for 6 months after injection than intra-articular corticosteroids . In an exploratory study, the effectiveness of intra-articular injections of a solution combining hyaluronic acid and chondroitin sulfate was assessed in 40 patients with knee osteoarthritis . The clinical improvement, together with the changes of the ultrasound parameters and biomarkers of cartilage metabolism and joint inflammation, suggested a non-placebo effect. These results prompted us to assess in a prospective multicenter study the effectiveness and safety of the use of hyaluronic acid when combined with chondroitin sulfate in patients with knee osteoarthritis.
Materials and methods
This was an open, multicenter, prospective study, assessing the effectiveness of three intra-articular injections of sodium hyaluronate plus chondroitin sulfate (40 mg of each compound in 2 mL) in the symptomatic treatment of knee osteoarthritis.
The study was conducted prospectively by office or hospital specialists (orthopedic surgeons, rehabilitation medicine physicians) from October 2012 to December 2013.
Written informed consent was obtained from each patient. The protocol was conducted in accordance with the Declaration of Helsinki and Guidelines on Good Clinical Practice and approved by a local ethics committee.
Men or women over 40 years of age were eligible to participate if they: (1) had documented knee osteoarthritis evidenced with X-rays over the past 6 months with Kellgren-Lawrence score grade II or III ; (2) had pain and functional impairment for at least 3 months and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)  subscore A (severity of pain) ≥25 (on a scale of 100); and (3) needed hyaluronic acid injections after the failure or intolerance to first-line analgesics or non steroidal anti-inflammatory drugs. The main exclusion criteria were: severe hydrarthrosis; inflammatory rheumatism; history of knee trauma in the past 6 months; history of arthroplasty or major surgery on the target knee in the past 6 months; history of arthroscopy or surgery on the target knee in the past 3 months; planned knee surgery during the study; history of septic arthritis of the knee; knee wound or skin condition; crural or sciatic radiculalgia of the lower limb; tendinopathy; symptomatic homolateral or contralateral hip disease; venous or lymphatic stenosis of the lower limb; medical history of venous thromboembolism (including pulmonary embolism) or patient with high risk of venous thromboembolism; patient with a history of auto-immune disease; treatment with diacerein, avocado soy unsaponifiables, glucosamine sulfate/chondroitin starting less than 3 months previously or with dosage modified during the past 3 months; recurrent episodes of chondrocalcinosis; previous treatment with viscosupplementation; injection of corticosteroids into the knee under study less than 3 months previously; known hypersensitivity to hyaluronic acid or substances with similar activity; ongoing anticoagulant therapy; pregnant or breastfeeding women.
Treatment and clinical assessments
Demographic, description and history of knee osteoarthritis, concomitant treatments and WOMAC subscore A were recorded at inclusion visit. The WOMAC (Western Ontario and McMaster Universities) index is used to assess patients with osteoarthritis of the hip or knee . The subscore A of the index is for pain assessment in five different circumstances: during walking (A1), using stairs (A2), in bed (A3), sitting or lying (A4) and standing (A5). For each item, pain is graded from 0 (none) to 100 (extreme). The sum for the five items is divided by five to give WOMAC subscore A.
Patients received three intra-articular injections of Arthrum HCS® (40 mg hyaluronic acid and 40 mg chondroitin sulfate in 2 mL) 1 week apart. Assessment of treatment effectiveness and safety was performed during follow-up visits at 1 month, 3 months and 6 months after the last intra-articular injection.
The effectiveness assessment during the follow-up visits included: WOMAC subscore A, relief of pain using a visual analogic scale (VAS) ranging from 0 (“maximum relief”, i.e., no pain) to 100 (“no relief”, i.e., maximal pain) and consumption of analgesic drugs using a VAS ranging from 0 (“no consumption of analgesics”) to 100 (“maximal consumption of analgesics)”.
Adverse events were recorded immediately after the injections and during the follow-up visits.
Data from previous studies were used to estimate the sample size [22, 23] With a loss to follow-up equal to 10 %, it was estimated that a sample size of 122 patients would provide 50 % power to detect a significant change of WOMAC subscore A (with alpha-risk at 5 %).
The primary endpoint was the change of WOMAC subscore A from inclusion to end of study. The secondary endpoints were the change of WOMAC subscore A from inclusion to month 1 or month 3, relief of pain at months 1, 3 and 6, consumption of analgesic drugs from baseline to months 1, 3 and 6 and global assessment by the investigator at the end of the study for the three criteria: pain reduction, improved mobility and consumption of analgesics.
Comparisons were made using Student’s t test for quantitative criteria and Chi2 test for non-ordinal qualitative variables (or Fisher’s exact test) and Wilcoxon’s test for ordinal data. The threshold for significance was set at 5 %.
The analyses were performed using SAS version 9.2 (SAS Institute, Cary, NC).
Among 132 screened patients, 112 were analyzed (20 patients were <40 years of age and/or had a WOMAC subscore A <25).
Characteristics of patients at inclusion
N = 112
Female gender, n (%)
Body mass indexa (kg/m2)
Study knee, n (%)
67 (59.8 %)
44 (3.3 %)
Right and left
1 (0.9 %)
Duration of knee osteoarthritisb, years, mean (SD)
Radiological stage, n (%)
64 (57.1 %)
48 (42.9 %)
Prior knee surgeryb n (%)
29 (27.9 %)
Prior physical medicine and rehabilitationc
48 (43.6 %)
At least one analgesic drug within 3 months
87 (77.7 %)
The mean duration of knee osteoarthritis was 3 years; 27.9 % (29/104) of patients underwent knee surgery (the main operation was meniscectomy; 35.7 %, 10/28). The median time between operation and inclusion was 7 years (n = 28). Just under half of patients had benefited from physical treatment and rehabilitation medicine (43.6 %; 48/110).
About four out of five patients (77.7 %; 87/112) were taking at least one analgesic treatment during the 3 months prior to the intra-articular injections: NSAIDs for 74.1 % (83/112) of patients and an analgesic other than NSAIDs for 34.9 % (38/109) of patients. There was a moderate relief due to the analgesic treatment: on a VAS from 0 (no relief) to 100 (maximal relief), the mean relief due to the analgesic treatment was 50.8 and 53.9 according to the investigator and the patient (n = 87), respectively.
Severity of pain—WOMAC subscore A
On inclusion, the mean WOMAC subscore A was 52.1 (range 26–86). At 6 months, the mean WOMAC subscore A was 20.5 (range 0–80). Thus, the decrease of the subscore was −31.4 (P < 0.0001; Wilcoxon signed rank test).
Pain severity (WOMAC subscore A) after three intra-articular injections of sodium hyaluronate-chondroitin sulfate. Results are given as mean (SD). For each item, pain is graded from 0 (none) to 100 (extreme)
Items of WOMAC A
A2 (using stairs)
A3 (in bed)
A4 (sitting or lying)
One month after the last intra-articular injection, the mean pain relief was assessed at 35.9 (25.6) on VAS by patients (0, maximal pain relief; 100, no relief). Pain relief continued to decrease at 3 and 6 months: 28.1 (23.1) and 26.1 (25.4), respectively. Compared to the values at 1 month, the values of pain relief at 3 and 6 months were statistically significant (P < 0.0001 and P = 0.0048, respectively).
Consumption of analgesic drugs
One month after the last intra-articular injection, the patients assessed on a VAS their mean consumption of analgesic drugs from 0 (no consumption of analgesics) to 100 (maximal consumption of analgesics). The mean (SD) consumption decreased with time: 28.6 (24.4) at 1 month, 19.9 (21.7) at 3 months and 17.1 (22.3) at 6 months. Compared to the values at 1 month, the scores of the consumption of analgesic drugs at 3 and 6 months were significantly decreased (P < 0.0001 for both times).
Global assessment by investigators
Overall, about 80 % of investigators stated that the results of the intra-articular injections of sodium hyaluronate-chondroitin sulfate combination were satisfactory or very satisfactory.
One adverse effect was reported by one patient. This adverse event was knee tumefaction, which lasted 3 days after the first intra-articular injection.
Viscosupplementation with hyaluronic acid alone has demonstrated moderate but significant effectiveness vs placebo in terms of pain and function in knee osteoarthritis . Our study is the first, to our knowledge, to assess the effectiveness and safety of injections of Arthrum HCS® in a relatively large population of patients with knee osteoarthritis. We observed that the severity of pain assessed with the WOMAC subscore A decreased significantly from 52.1 to 20.5 at 6 months. The relief was already significant 1 month after the last injection. These results were confirmed by the assessment of pain relief and the decrease in the consumption of analgesics with VAS. Approximately three out of four investigators were satisfied/very satisfied as regards to the therapeutic effectiveness of the injections of sodium hyaluronate-chondroitin sulfate in reducing pain, improving mobility and reducing the consumption of analgesics.
The pilot study of Maheu et al.  in 41 patients with femoro-tibial knee osteoarthritis also reported an improvement 3 months after three 2-mL injections of hyaluronic acid (12 mg/mL) plus chondroitin sulfate (30 mg/mL). The mean VAS score decreased from 61 at baseline to 29 after 3 months (60 % of patients reported an improvement above 50 %). Although the dosages of the compounds were slightly different, these results are consistent with those of the present study.
The very low proportion of patients with adverse events confirms the safety of viscosupplementation in knee osteoarthritis. The harmlessness of viscosupplementation in knee osteoarthritis has been confirmed in a recent systematic review and meta-analysis of randomized saline-controlled trials for US-approved intra-articular hyaluronic acid . There were no statistically significant differences between hyaluronic acid and saline controls for any safety outcome.
It is now debated that surgical procedures in knee osteoarthritis should be avoided as far as possible or at least delayed [25, 26]. The restoration of the viscoelasticity of the synovial fluid in order to protect cartilage, if possible during the early states of the disease, is an attractive therapeutic option. Moreover, a medico-economic evaluation showed that, together with clinical benefits, costs of knee osteoarthritis decreased after hyaluronic acid injections due to the decreased need for other treatments . However no therapies have been shown to alter the natural history of osteoarthritis. In the absence of disease modifying osteoarthritis drugs, treatment of osteoarthritis is focused on controlling symptoms, especially pain [10, 27, 28]. Until prospective studies on the efficacy of hyaluronic acid on knee arthroplasty delay are completed, intra-articular treatment must be considered an additional non-operative strategy for relief of symptoms.
There are some limitations of the study. First, there was no control group. Indeed, there is a debate on the effectiveness of viscosupplementation in osteoarthritis, but some meta-analyses found an advantage of viscosupplementation over sham intervention [14, 24, 25]. Therefore, it was difficult to justify a sham control in one group. Nevertheless, the kinetics of the effect observed in the present study conform to the conclusions of a meta-analysis on viscosupplementation that showed that effectiveness became significant at 4 weeks, peaked at 8 weeks and persisted for 6 months . Another limitation was the absence of demonstration of the benefit of the addition of chondroitin sulfate to hyaluronic acid. With a comparable total number of patients, the statistical power of the trial would decrease with an additional treatment group (hyaluronic acid alone). This issue should certainly be addressed in further studies.
Arthrum HCS® is a new intra-articular treatment combining in the same injection two compounds that are deficient in osteoarthritis. Chondroitin sulfate is an essential component of cartilage and is present also in synovial fluid. Our results suggest that intra-articular injections of Arthrum HCS® (sodium hyaluronate plus chondroitin sulfate) in patients with knee osteoarthritis allows a safe and effective control of pain. These results should be confirmed in a randomized controlled study.
Compliance with ethical standards
Conflict of interest
All authors received a consultancy fee reimbursement from LCA Pharmaceutical, Chartres, France, to contribute to completing this study. This research received no specific grant from any funding agency in the public, or not-for-profit sectors.
All patients gave informed consent prior being included into the study. All procedures involving human participants were in accordance with the 1964 Helsinki Declaration and its later amendments. The study was approved by the Research Ethics Committee.
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