display ongoing studies | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Study | Ref. | Design | studied treatment | control treatment | patients | study risk of bias | sample sizes | Results | symptomatic Covid-19 E | new illness compatible with Covid-19 E | conversion to SARS-CoV- 2–positive status via NP swab E | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
COVID 19 outpatients meta-analysis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
PINETREE (GS-US-540-9012) NCT04501952 | RCT | remdesivir | placebo | COVID 19 outpatients | low | 292/292 | conclusif |
PE: primary endpoint; (a): to be demonstrated a result must be statistically significant on a primary endpoint (with multiplicity adjustment if necessary);
Study risk of bias assessed for the study primary endpoint(s) or the main endpoints in case of no formally defined primary endpoint(s).