Kitamoto 1971.
Methods | Randomised, double‐blind, placebo controlled treatment trial of oral amantadine. The trial took place during the 1968 to 1969 influenza season throughout Japan | |
Participants | 79 participants were randomised to receive amantadine (200 mg/day for adults) and 76 placebo for 7 days within 48 hours of developing symptoms | |
Interventions | Amantadine and placebo in a treatment role | |
Outcomes | Case definition was based on symptoms and serological confirmation of infection. Outcomes were duration of fever (in days), defined as a temperature of more that 37 degrees centigrade and there were no drop‐outs from the study Safety: adverse events were reported as nil |
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Notes | Although randomisation was clearly applied and no drop‐outs are reported, no description of allocation and concealment is given making its assessment impossible. In addition the follow up of 353 participants is unclear. The authors conclude that treatment started within 2 days of symptom onset shortened significantly the duration of illness and of high fever but did not affect asymptomatic influenza | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment (selection bias) | Unclear risk | B ‐ Unclear |