Trial Analysis
Cross-source consensus on Trial Analysis from 1 sources and 4 claims.
1 sources · 4 claims
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Highlighted claims
- An interim analysis is planned after 45 participants are recruited. — Unbound cloxacillin plasma concentrations in relation to toxicity and renal function: protocol for a prospective, observational clinical trial in a real-world Staphylococcus aureus bacteraemia population
- The sample size is primarily designed for analyses involving renal function. — Unbound cloxacillin plasma concentrations in relation to toxicity and renal function: protocol for a prospective, observational clinical trial in a real-world Staphylococcus aureus bacteraemia population
- The trial requires at least 95 participants split across predefined renal function groups. — Unbound cloxacillin plasma concentrations in relation to toxicity and renal function: protocol for a prospective, observational clinical trial in a real-world Staphylococcus aureus bacteraemia population
- Primary endpoints are analysed using univariate logistic regression and receiver operating characteristic curves. — Unbound cloxacillin plasma concentrations in relation to toxicity and renal function: protocol for a prospective, observational clinical trial in a real-world Staphylococcus aureus bacteraemia population