There are few effective treatments for acute whiplash-associated disorders (WADs). Early features of central sensitisation predict poor recovery. The effect of
pregabalin on central sensitisation might prevent
chronic pain after acute
whiplash injury. This double blind, placebo-controlled randomised controlled trial examined feasibility and potential effectiveness of
pregabalin compared with placebo for people with acute WAD. Twenty-four participants with acute WAD (<48 hours) and at risk of poor recovery (
pain ≥5/10) were recruited from hospital emergency departments in Queensland, Australia, and randomly assigned by concealed allocation to either
pregabalin (n = 10) or placebo (n = 14).
Pregabalin was commenced at 75 mg bd, titrated to 300 mg bd for 4 weeks, and then weaned over 1 week. Participants were assessed at 5 weeks and 3, 6, and 12 months. Feasibility issues included recruitment difficulties and greater attrition in the placebo group. For the primary clinical outcome of
neck pain intensity, attrition at 5 weeks was
pregabalin: 10% and placebo: 36% and at 12 months was
pregabalin: 10% and placebo: 43%.
Pregabalin may be more effective than placebo for the primary clinical outcome of
neck pain intensity at 3 months (mean difference: -4.0 [95% confidence interval -6.2 to -1.7]) on an 11-point Numerical Rating Scale. Effects were maintained at 6 months but not 12 months. There were no serious adverse events. Minor adverse events were more common in the
pregabalin group. A definitive large randomised controlled trial of
pregabalin for acute
whiplash injury is warranted. Feasibility issues would need to be addressed with modifications to the protocol.