Nafta 1970.
Methods | Randomised, double‐blind, placebo controlled prevention trial of amantadine during the 1969 Hong Kong influenza epidemic in 4 locations in Romania (2 sanatoria, 1 blood transfusion centre and 1 public health department). Treatment was started before influenza activity was recognised. Randomisation is not described but both drugs and placebo were centrally prepared and were indistinguishable apart from a letter C for the active principle and R for placebo | |
Participants | 215 healthy subjects in the 4 trial locations. No withdrawals are reported. Data are reported for all participants by pre‐treatment serological status and study site | |
Interventions | Oral placebo or amantadine 100 mg twice daily for 20 days | |
Outcomes | Serological/laboratory: antibody response with paired sera (fourfold or more increase was considered positive) Effectiveness: cases of influenza Cases of ILI (influenza symptoms but no antibody rise) Antibody rise with no influenza symptoms Safety: no adverse events are reported |
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Notes | The authors conclude that amantadine was highly effective in preventing influenza from Hong/Kong A2 virus and appeared to prevent symptom expression without interfering with the immune response. A well‐reported trial. We assume all participants were healthy |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment (selection bias) | Unclear risk | B ‐ Unclear |