Topical treatments for scalp psoriasis Background: People with chronic plaque psoriasis often have lesions on the scalp that are difficult to treat. Our objective was to assess the efficacy and safety of topical treatments for scalp psoriasis. Methods: We searched the following databases up to August 2015: the Cochrane Skin Group Specialised Register, CENTRAL, MEDLINE, EMBASE and LILACS. We also searched five trial registers, screened abstracts of six psoriasis-specific conferences and checked the bibliography of included studies for further references to relevant randomised controlled trials (RCTs). Our quality of evidence assessment was based on the Grading of Recommendations Assessment, Development and Evaluation (GRADE) Working Group approach. We graded the quality of evidence for the following outcomes: 'clearance' or 'response' as assessed by the investigator global assessment (IGA) and 'response' according to the patient global assessment (PGA), improvement in quality of life, and the number of patients with adverse events (AE) requiring withdrawal of treatment. We expressed the results of the individual studies as risk ratios (RR) with 95% confidence intervals (CI) for dichotomous outcomes, and mean differences with 95% CI for continuous outcomes. If studies were sufficiently homogeneous, we metaanalysed the data by using the random-effects model. Results: We included 59 RCTs, with overall 11.561 participants. Most findings were limited to short-term treatments (< six months). Overall evidence was of moderate quality. According to the clinician and patients' self-assessment a corticosteroid/vitamin D combination (e.g. betamethasone dipropionate plus calcipotriol) and corticosteroids of high and very high potency were more effective than vitamin D. The two-compound combination was superior to the corticosteroid alone, but the additional benefit was small. Reporting of quality of life data was insufficient to be included for meta-analyses and not feasible for quality of evidence assessment. The two-compound combination and corticosteroids caused fewer withdrawals due to AEs than vitamin D. There was no difference between the two-compound combination and corticosteroid monotherapy concerning this outcome. None of the studies stated which AE that caused withdrawal from treatment. However, the risk of withdrawing due to AEs was very small for all three therapies. Due to poor data evaluation of most other topical treatments was limited.