A Cochrane review included 11 studies with a total of 1019 participants who received tramadol or tramadol/paracetamol and 920 participants who received placebo or active control. Patients who received tramadol had less pain (–8.5 units on a 0 to 100 scale; 95% confidence interval [CI] –12.0 to –5.0) than patients who received placebo. With tramadol there was a 37% increase (95% CI 1.2 to 1.5) in the likelihood of reporting moderate improvement (NNT = 6; 95% CI 4 to 9). The risk of minor adverse events was 2.27 times and the risk of major adverse events 2.6 times higher with tramadol than with placebo. Number needed to harm (NNH; stopping of tramadol or tramadol/paracetamol medication for major adverse events) = 8 (95% CI 7 to 12).
No conclusion could be drawn on tramadol or tramadol/paracetamol compared with other available pharmacological treatments because of limited number of studies.