Table 1.

Risk of bias assessment for the included studies

Ruby, 19737Zaynoun, 19748Eells, 19869Koning, 200210Koning, 200811Gropper, 201412Rosen, 201813
Defined sample: description of source of patients and inclusion and exclusion criteriaHospital outpatient clinic. Describes some exclusion criteria, but not inclusion criteriaHospital outpatient clinic. Does not describe inclusion or exclusion criteriaNo mention of where trial was conducted. Describes inclusion and exclusion criteriaGeneral practices. Describes inclusion and exclusion criteria‘General practices and dermatology departments’. Describes inclusion and exclusion criteriaUnclear patient source: ‘27 centres in five countries’. Mentions ‘clinic visits’. Describes inclusion and exclusion criteriaUnclear patient source: multicountry and multicentre trial at various sites (clinic, hospital). Describes inclusion and exclusion criteria
Representative sample: participants were selected as consecutive casesNRNRNRNRNRNRNR
Follow-up rate: outcome data available for ≤80% of participants at one follow-up pointNRYesYesYes79% (n = 58/73) on day 14, per-protocolYesYes (but unequal loss between groups; more loss in placebo group)
Prognosis: raw data, percentages, survival rates, or continuous outcomes reportedYesYesYesYesYesYesYes
  • NR = not reported.