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01.08.2008 | Knee | Ausgabe 8/2008 Open Access

Knee Surgery, Sports Traumatology, Arthroscopy 8/2008

Multicentre, prospective, open study to evaluate the safety and efficacy of hylan G-F 20 in knee osteoarthritis subjects presenting with pain following arthroscopic meniscectomy

Knee Surgery, Sports Traumatology, Arthroscopy > Ausgabe 8/2008
J. P. Huskin, B. Vandekerckhove, P. Delincé, R. Verdonk, J.-E. Dubuc, S. Willems, P. Hardy, F. J. Blanco, O. Charrois, F. Handelberg


Osteoarthritis (OA) is a chronic, degenerative disorder associated with joint pain and loss of joint function. It is the most common disease to affect synovial joints and is one of the most frequently occurring chronic conditions.
The primary goal of treatment is the alleviation of pain, leading to an improvement in joint function and quality of life. Treatment options for knee OA include conservative therapies (education, weight loss, physical therapy, etc.), pharmacological therapies (simple analgesics, NSAIDs (including COX-2s)), intra-articular injections (corticosteroids, viscosupplements) and surgical intervention (e.g. arthroscopic debridement and lavage, meniscectomy, total knee replacement (TKR)).
More than 90% of patients with symptomatic OA of the knee have evidence of meniscal tears on magnetic resonance imaging [ 6], and arthroscopic meniscectomy can be used to treat patients who are unresponsive to more conservative therapies, but are not yet TKR candidates. However, the clinical benefit of arthroscopic debridement is unclear. In a double-blind study, Moseley et al. [ 11] randomised 180 patients who underwent arthroscopic debridement, arthroscopic lavage, or placebo surgery. At no point during the 24-month follow-up did either of the intervention groups report less pain or better function than the placebo group. In contrast, Matsusue [ 10] reported that 87% of patients with grade I or II OA achieved “excellent” symptomatic relief from meniscal tear debridement. Until such time as there is consensus on the clinical benefit of arthroscopic intervention for OA, it is likely that it will remain in the orthopaedic armamentarium. However, a sub-set of post-operative patients who have not gained adequate symptomatic relief will continue to present with persistent osteoarthritic pain several weeks or months after the procedure. The causative factors behind this persistent pain are unknown, but it is likely that the severity and extent of OA, the degree of debridement performed and the skill of the surgeon are major factors.
Viscosupplementation (intra-articular supplementation of hyaluronic acid) is a well-established treatment option in knee OA and is included in the professional guidelines for treatment of the disease in this joint [ 2, 12] Several meta-analyses have been conducted on the therapy class, which agree broadly that viscosupplementation is effective and safe [ 3, 5, 16].
Hylan G-F 20 (Synvisc ©, Genzyme Corporation, MA, USA) is a high molecular weight, cross-linked derivative of hyaluronan. The safety and efficacy of viscosupplementation with hylan G-F 20 in OA of the knee is supported by prospective clinical trials [ 1, 13, 14, 17] and large retrospective studies [ 8, 15].
The use of viscosupplementation for the symptomatic relief of knee OA in patients after arthroscopic meniscectomy has not been widely studied. Marshall [ 9] reported on a retrospective series of 92 patients treated with hylan G-F 20 after failing conservative treatments and standardised arthroscopic debridement and injection of IA steroid. The majority of these patients (77%) had “marked” or “severe” OA; 68% of patients did not go on to TKR during the 2.5 year follow-up and were considered as “salvaged”.
This study aimed to assess the efficacy and safety of viscosupplementation with hylan G-F 20 in patients with mild or moderate knee OA who had failed to achieve adequate symptomatic relief from arthroscopic meniscectomy.

Materials and methods


Patients were enrolled at 10 centres across Europe: Belgium (7), France (2) and Spain. The study protocol, patient information and patient consent form were approved by the independent ethics committee of each investigating centre. Written, informed consent was obtained from each patient prior to enrolment in the study.
To be considered eligible for inclusion, patients had to present with osteoarthritic knee pain 4-12 weeks after arthroscopic meniscectomy (mean time from meniscectomy to the first injection of hylan G-F 20 was 53 days (range 27–107 days)) and must have had osteoarthritic cartilage lesion(s) observed during arthroscopy. The location and severity (Kellgren-Lawrence grade) of OA observed on baseline X-rays is shown in Fig.  1. Each arthroscopic surgery (Fig.  2) was performed by the authors, all skilled and experienced in this technique.
Patients were considered eligible for inclusion if they scored ≥50 mm and ≤90 mm on both the walking pain and patient global assessment visual analogue scales (VAS) (0–100 mm) at the screening visit. Patients were required to have X-ray evidence (pre-operative anteroposterior weight-bearing view (extension) + profile and patellofemoral at 30° classical (taken within 3 months of the arthroscopic meniscectomy)) of osteoarthritis of the knee (Kellgren-Lawrence grade I or II, <50% joint space narrowing).
The main exclusion criterion was any surgery on the cartilage during arthroscopic meniscectomy, except for non-therapeutic, superficial mechanical shaving of fibrillations and/or resection of unstable flaps in grade 2 and 3 lesions (grade 4 lesions were excluded), performed solely for the purpose of cleaning the area to enable accurate grading of the defect. Other exclusion criteria were: significant mechanical deficit (e.g. valgus/varus > 5%); symptomatic contralateral knee OA; concomitant inflammatory joint disease (e.g. gout, rheumatoid arthritis); history of sepsis in any joint; prior viscosupplementation in the target knee; oral and/or parenteral glucocorticosteroids or intra-articular corticosteroids in any joint within 3 months prior to enrolment.

Trial design

This was a prospective, multi-centre, open study conducted between February 2002 and March 2005. A washout period of 1–3 weeks was applied (adapted to half-life), commencing at the screening visit, if patients had been taking prohibited analgesic medications. Once any required washout was completed and eligibility confirmed, patients presented for the baseline visit and received a single intra-articular 2 ml injection of hylan G-F 20 using a strict aseptic administration technique. Prior to each injection, arthrocentesis was performed carefully, without injecting local anaesthetic into the joint space, to remove any effusion present. The suggested injection site was the lateral tibiofemoral joint space in the extended knee.
No standard rehabilitation protocol was imposed. Medication for pre-existing conditions was permitted. Also permitted were: paracetamol (≤4 g/day) except on the day before and on the day of the follow-up visits; analgesics and NSAIDs, other than COX-2 inhibitors, with a clearance time of <8 h for pain other than OA in the study knee, or for post-injection pain management, but not on the day before or on the day of a study visit; aspirin (≤ 325 mg/day) for anti-thrombotic prophylaxis; topical corticosteroids for skin problems, except at the study knee; inhaled corticosteroids for asthma and allergic disease; non-pharmacological therapy (e.g. physical therapy) if begun before the study entry.
Prohibited medications were: analgesics and aspirin except as described above; COX-2 inhibitors; oral or parenteral corticosteroids; corticosteroid injections in any joint; topical analgesics at the study knee; therapeutic treatment with oral or parenteral anticoagulants. Chondroprotective agents were not prohibited, but were not used by any of the patients in the study. The use of all rescue and concomitant medications and therapies were recorded in the patient notes.
Patients returned to the investigational site at week 1 and week 2 for the remaining two injections of hylan G-F 20, and for follow-up and safety evaluations at week 12, 26 and 52. At each visit, walking pain, physician global assessment and patient global assessment VAS were completed, the WOMAC™ questionnaire was filled out by the patient, and concomitant therapy and adverse events were recorded.

Outcome measures

All efficacy analyses were performed on the intent-to-treat (ITT) population, which was defined as those patients who received at least one injection and for whom post-baseline efficacy data were present for at least the walking pain VAS. The primary efficacy outcome measure was the change from baseline in walking pain VAS at 26 weeks. Secondary efficacy outcome measures were: change from baseline in walking pain VAS at all other follow-up visits; change from baseline in WOMAC osteoarthritis index scores (pain (A), stiffness (B), physical functioning (C) and composite scores) at all time points; change from baseline in patient and physician global assessment VAS scores at all time points.
The safety assessment was based on reports of adverse events (AEs) collected between the signing of the informed consent form and the completion of the final follow-up visit for each patient.



The ITT population consisted of 62 patients. During the study, seven patients were lost to follow-up, six withdrew due to target knee AEs, two became ineligible to continue, one withdrew consent and three patients discontinued from the study for other reasons. A total of 43 patients (69%) completed the study. Baseline demographics for the ITT population are presented in Table  1.
Table 1
Demographic data (ITT population)
ITT population
Number of patients
Gender: male/female, n (%)
32/30 (52/48)
Age (years): mean (SD)
55.4 (11.35)
Weight (kg): mean (SD)
81.6 (14.97)
Height (cm): mean (SD)
168.8 (9.64)
Body mass index (kg/m 2): mean (SD)
28.9 (6.26)

Primary efficacy endpoint

There was a statistically significant decrease in the mean score of the walking pain VAS from 65.0 mm at baseline to 28.0 at week 26 ( P < 0.0001; Fig.  3).

Secondary efficacy endpoints

Walking pain VAS

The decreases from baseline in the walking pain VAS were statistically significant ( P < 0.0001) at all time points (Fig.  3).


Changes from baseline in the mean WOMAC scores (A, B, C and composite) were statistically significant ( P < 0.0001) at all time points (Fig.  4).

Patient and physician global assessment

Changes from baseline in the mean patient and physician global assessment scores were statistically significant at all time points ( P < 0.0001; Fig.  5).


Twelve patients (19%) reported a total of 18 target knee AEs (arthralgia, joint swelling and joint effusion) that were considered possibly (10 AEs) or probably (8 AEs) related to the study treatment. These AEs were mostly considered to be mild (1 AE) or moderate (13 AEs) in severity. One serious target knee AE (“synovitis” i.e. pain and swelling, which developed more than 2 months after the last injection of hylan G-F 20) was reported during the study and was considered possibly related to the study treatment.
Three patients discontinued the study due to the occurrence of target knee AEs considered possibly or probably study treatment related.


This is the first study to evaluate prospectively the efficacy and safety of intra-articular injections of hylan G-F 20 in patients with symptomatic knee OA unresponsive to simple analgesics 4-12 weeks after arthroscopic meniscectomy.
Although definitive conclusions about efficacy cannot be drawn from this study due to its open label design, hylan G-F 20 was effective at significantly reducing the pain associated with knee OA. Statistically significant changes from baseline were seen consistently in all primary and secondary efficacy outcome measures at all time points.
In the ITT population, reduction in pain was apparent from as soon as 7 days after injection, was maximised at 12 weeks and maintained at 26 and 52 weeks. These results reflect those reported in other studies in patients with knee OA, where the symptomatic relief obtained by patients outlasts substantially the product’s residence time in the joint, thus supporting the hypothesis that viscosupplementation achieves its therapeutic effect by restoring the rheology of the joint temporarily [ 4].
The safety profile of hylan G-F 20 in knee OA is already supported by clinical literature. In the largest study conducted to date, Kemper et al. [ 7] assessed the safety of the treatment in 4,253 patients and reported AE rates of 4.2% of patients and 2.4% of injections. The types of AEs seen in our study were consistent with those seen in Kemper et al. and described in the product labelling (transient post-injection pain and/or swelling and/or effusion). The reason for the higher incidence of these AEs observed in this particular population of patients compared to previously published data is unknown. However, no new safety concerns were raised in this study and most AEs experienced were transient and of mild or moderate intensity.
We conclude that viscosupplementation with hylan G-F 20 has a favourable risk/benefit profile in patients with symptomatic knee OA presenting with persistent pain after arthroscopic meniscectomy.


This study was sponsored by Genzyme Europe B.V.

Conflict of interest statement

There are no conflicts of interest.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License ( https://​creativecommons.​org/​licenses/​by-nc/​2.​0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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