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 |