Tendon disorders comprise 30% to 50% of all activity-related injuries; chronic degenerative
tendon disorders (tendinopathy) occur frequently and are difficult to treat. Tendon
regeneration might be improved by injecting platelet-rich plasma (PRP), an increasingly
used treatment for releasing growth factors into the degenerative tendon.
To examine whether a PRP injection would improve outcome in chronic midportion Achilles
tendinopathy.
A stratified, block-randomized, double-blind, placebo-controlled trial at a single
center (The Hague Medical Center, Leidschendam, The Netherlands) of 54 randomized
patients aged 18 to 70 years with chronic tendinopathy 2 to 7 cm above the Achilles
tendon insertion. The trial was conducted between August 28, 2008, and January 29,
2009, with follow-up until July 16, 2009.
Eccentric exercises (usual care) with either a PRP injection (PRP group) or saline
injection (placebo group). Randomization was stratified by activity level.
The validated Victorian Institute of Sports Assessment-Achilles (VISA-A) questionnaire,
which evaluated pain score and activity level, was completed at baseline and 6, 12,
and 24 weeks. The VISA-A score ranged from 0 to 100, with higher scores corresponding
with less pain and increased activity. Treatment group effects were evaluated using
general linear models on the basis of intention-to-treat.
After randomization into the PRP group (n = 27) or placebo group (n = 27), there was
complete follow-up of all patients. The mean VISA-A score improved significantly after
24 weeks in the PRP group by 21.7 points (95% confidence interval [CI], 13.0-30.5)
and in the placebo group by 20.5 points (95% CI, 11.6-29.4). The increase was not
significantly different between both groups (adjusted between-group difference from
baseline to 24 weeks, -0.9; 95% CI, -12.4 to 10.6). This CI did not include the predefined
relevant difference of 12 points in favor of PRP treatment.
Among patients with chronic Achilles tendinopathy who were treated with eccentric
exercises, a PRP injection compared with a saline injection did not result in greater
improvement in pain and activity.
clinicaltrials.gov Identifier: NCT00761423.