Hand Osteoarthritis
Conditions
Keywords
Hand OA, Tocilizumab, Osteoarthritis, Interleukin-6
Brief summary
Hand osteoarthritis (HOA) which affects the interphalangeal joints and the metacarpophalangeal of the thumb is a common disease, the prevalence of which being about 30 % of the population over than 70. Some forms of HOA are refractory to usual treatments (analgesics, NSAIDs, local injections) and can lead to a high disability. In vitro and in vivo studies showed that IL-6 is involved in the OA process. The aim of the present study is to assess the efficacy of an Interleukin-6-Receptor Inhibitor (tocilizumab) on pain and function in patients with refractory hand OA.
Detailed description
Patient is randomized to receive investigational product or placebo at week 0 and week 4 (1:1) * arm 1: 2 infusions four weeks apart of tocilizumab 8mg/kg * arm 2: 2 infusions four weeks apart of saline solution Follow-up visits are organized at week 6, and then week 8 and week 12. Primary outcome is the pain as assessed with the VAS at week 6. Secondary outcomes include morning stiffness duration, patient and practitioner global assessments, functional indexes for hand OA, number of painful joints, number of swollen joints. 110 patients is expected to be randomized in 36 months. Each patient sign an informed consent before the beginning of the study.
Interventions
DRUGtocilizumab
Le tocilizumab is administered by intravenous infusion at a dose of 8 mg / kg.
DRUGsaline solution
La saline solution is administered by intravenous infusion.
Sponsors
Hoffmann-La Roche
Assistance Publique - Hôpitaux de Paris
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
40 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Age: 40-85 * Hand OA according to the ACR criteria (with recent X-rays of the hands - less than 6 months ) * Symptomatic hand OA lasting more than 3 months (DIP or PIP) despite analgesics and NSAIDs * OA affecting more than three finger joints (DIP or PIP) (Kellgren and Lawrence equal or more than 2) * Pain intensity superior to 40 (VAS 0-100 mm) in the last 24 hours * Not breastfeeding throughout the study and for 150 days after the last infusion * Negative pregnancy test or effective contraception for women of childbearing age throughout the study and for 150 days after the last infusion or postmenopausal or surgically sterile * Written informed consent * Affiliated to health system
Exclusion criteria
* Patients having already been treated with an anti-TNF alpha within 6 months * Patients having already been treated with an Interleukin-6-Receptor Inhibitor * Hand OA secondary to inflammatory rheumatism * Existence of painful syndrome of upper limbs likely to interfere with the monitoring of pain (cervicobrachial neuralgia, incapacitating carpal tunnel syndrome, joint disorders of the elbow or shoulder) * Inflammatory rheumatism * Psoriasis * Contraindications to Interleukin-6-Receptor Inhibitor * Contraindications to acetaminophen * Anticoagulant (oral) or treatment with heparin at a curative dose * Surgery scheduled within 6 months following recruitment * Local injection of a corticosteroid in a symptomatic finger joint during the previous month * Local injection of hyaluronic acid in a symptomatic finger joint during the prior 6 months * Treatment with a slow-acting anti-osteoarthritis agent initiated within the previous 3 months * Treatment with methotrexate, hydrochloroquine, sulfasalazine, colchicine within the last month * History of symptomatics sigmoiditis or intestinal ulceration * Oral corticosteroid within 3 days for hydrocortisone or cortisone, within 8 days for prednisone, prednisolone, methylprednisolone or triamcinolone, and within 12 days for betamethasone or dexamethasone * Psychiatric illness * Antidepressants initiated or modified within previous month * Non-controlled diabetes mellitus * Known viral hepatitis B or C, HIV infection * Current infectious (active or latent tuberculosis) * Excessive drinking * Participation in another search * Lidocain plasters on digital joint within two months
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of pain | 6 weeks | Change of pain between the first infusion (week 0) and 2 weeks after the second infusion (week 6) as assessed on the VAS (0 -100 mm) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of painful joints | weeks 4, 6, 8, 12 | — |
| Number of swollen joints | weeks 4, 6, 8, 12 | — |
| Change of pain | weeks 4, 8, 12 | Change of pain between the first infusion (week 0) and 4, 8,12 weeks after the first infusion as assessed on the VAS (0 -100 mm) |
| Morning stiffness duration | weeks 4, 6, 8, 12 | — |
| Evaluation of the function | weeks 4, 6, 8, 12 | Dreiser's algofunctional index + Functional Cochin hand index |
| Overall assessment of disability | weeks 4, 6, 8, 12 | Patient and practitioner global assessments |
Countries
France
Outcome results
None listed