Pm. Peloso et al., Double blind randomized placebo control trial of controlled release codeine in the treatment of osteoarthritis of the hip or knee, J RHEUMATOL, 27(3), 2000, pp. 764-771
Objective. Pain is the cardinal feature of osteoarthritis (OA), and with ad
vancing disease there is loss of function and increasing pain even at times
of joint rest, Few studies have evaluated the role of opioid analgesics in
treating the pain of OA.
Methods. This randomized, double blind, parallel group study compared the e
fficacy and safety of a 12 hourly controlled release codeine formulation (C
odeine Contin(R)) with placebo in patients with chronic pain due to QA of t
he hips and/or knees. The 4 week treatment period, following an analgesic w
ashout phase of 2-7 days, included weekly clinic evaluations, at which the
dose was escalated as appropriate, and daily patient diary completion. Pain
(daily), stiffness, and physical function (weekly) were assessed using the
multidimensional, self-administered WOMAC (visual analog scale version) qu
estionnaire.
Results. Sixty-six eligible patients completed the study. The mean initial
and final daily closes of controlled release codeine were 50 mg every 12 h
at baseline and 159 mg every 12 h at the final assessment. All variables in
the efficacy analysis indicated superiority of controlled release codeine
over placebo. The WOMAC pain scale showed an improvement of 44.8% over base
line in the controlled release codeine group compared with 12.3% taking pla
cebo (p = 0.0004). For the WOMAC stiffness and physical function scales the
improvements over baseline on controlled release codeine were 47.7% and 49
.3%, respectively compared with 17.0% and 17.0%, respectively, with placebo
(p = 0.003; p = 0.0007). Controlled release codeine was also significantly
better than placebo on measures of sleep quality and requirement for suppl
emental acetaminophen.
Conclusion, Single entity controlled release codeine is an effective treatm
ent for pain due to OA of the hip or knee.