Holti 1970.

Methods	RCT Study aim clearly defined: yes Blinded assessor of primary outcome: yes Double blind study: yes Participants comparable at baseline for age: not stated Sex: not stated Duration of complaint: not stated Inclusion and exclusion criteria specified: yes Interventions well described: yes Assessment of compliance: not stated Intention to treat analysis: not stated A Priori sample size calculation: not stated Fungi identified: yes Distribution of species between groups: yes Adverse events reported: yes Number of drop outs stated: not stated
Participants	Total evaluable sample size: 12 Treatment setting: multicentre
Interventions	a. Whitfields ointment Duration: eight weeks Frequency: once daily b. Varotin ointment Duration: eight weeks Frequency: once daily
Outcomes	Primary outcome: cure Adverse events: none
Notes
Risk of bias
Bias	Authors' judgement	Support for judgement
Allocation concealment (selection bias)	Unclear risk	B ‐ Unclear