Objective To systematically review the efficacy and safety of CoenzymeQ10 for Parkinson’s disease. Methods Databases including PubMed, The Cochrane Library (Issue 1, 2015), EMbase, CBM, CNKI, WanFang Data and VIP were searched from inception to August 2015, to collect randomized controlled trials (RCTs) about CoenzymeQ10 for Parkinson’s disease. Two reviewers independently screened literature, extracted data and assessed the risk of bias of included studies. Then meta-analysis was performed using RevMan 5.3 software. Results A total of 5 RCTs involving 981 patients were included. The results of meta-analysis showed that, a) As for recently effectiveness, CoenzymeQ10 2 400 mg group was superior to the placebo group in total UPDRS score change (MD=1.09, 95%CI 0.94 to 1.24, P < 0.000 01), UPDRS-I score change (MD=0.19, 95%CI 0.17 to 0.21, P < 0.000 01), UPDRS-II score change (MD=0.27, 95%CI 0.21 to 0.32, P < 0.000 01), UPDRS-III score change (MD=0.65, 95%CI 0.54 to 0.76, P < 0.000 01), Hoehn & Yahr score change (MD=0.05, 95%CI 0.04 to 0.06, P < 0.000 01), and Schwab England score change (MD= –0.87, 95%CI –1.02 to –0.72, P < 0.000 01). b) As for long-term effectiveness, there were no differences between two groups, except that the UPDRS-II score change of CoenzymeQ10 1 200 mg group was superior to the placebo group. c) As for adverse reactions, there were no statistical differences between two groups except that the incidence of cholesterol of the CoenzymeQ10 600 mg group and incidence of diarrhea of the CoenzymeQ10 2 400 mg group were lower than that of the placebo group. Conclusion Current evidence shows that, the dosage of 2 400 mg/d CoenzymeQ10 is effective and safe for early Parkinson’s disease. Due to the limited quality and quantity of included studies, more higher quality studies are needed to verify the above conclusion.