Pages that link to "Item:Q118080"
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The following pages link to Sample Sizes Based on the Log-Rank Statistic in Complex Clinical Trials (Q118080):
Displaying 21 items.
- nphPower (Q118083) (← links)
- The effect of grouping on the power of the Mantel-Haenszel test for the comparison of survival rates (Q1209444) (← links)
- Data monitoring in complex clinical trials: Which treatment is ''better''? (Q1338366) (← links)
- Sample size calculation for the proportional hazards model with a time-dependent covariate (Q1623465) (← links)
- A comparison of the constant piecewise weighted logrank and Fleming-Harrington tests (Q2015163) (← links)
- Sample size calculation for clustered survival data under subunit randomization (Q2126045) (← links)
- Cross-product ratio calculation under different sampling schemes in clinical trials -- case study of the CYP-GUIDES trial (Q2680680) (← links)
- Calculation of Sample Size in Survival Trials: The Impact of Informative Noncompliance (Q3445311) (← links)
- Sample size selection in clinical trials when population means are subject to a partial order: one-sided ordered alternatives (Q3532695) (← links)
- A note on variance estimation in the Cox proportional hazards model (Q5129000) (← links)
- A simple procedure to estimate the optimal sample size in case of conjunctive coprimary endpoints (Q5280177) (← links)
- The Influence of Biostatistics at the National Heart, Lung, and Blood Institute (Q5885361) (← links)
- Sample size calculation for two‐arm trials with time‐to‐event endpoint for nonproportional hazards using the concept of Relative Time when inference is built on comparing Weibull distributions (Q6085898) (← links)
- Sample size calculation for the combination test under nonproportional hazards (Q6143320) (← links)
- Designing a phase-III time-to-event clinical trial using a modified sample size formula and Poisson-Gamma model for subject accrual that accounts for the lag in site initiation using the PERT distribution (Q6560575) (← links)
- Assurance methods for designing a clinical trial with a delayed treatment effect (Q6618366) (← links)
- Complex survival trial design by the product integration method (Q6622288) (← links)
- Sequential trials in the context of competing risks: concepts and case study, with R and SAS code (Q6625156) (← links)
- Design and monitoring of survival trials in complex scenarios (Q6625542) (← links)
- Novel application of a discrete time-to-event model for randomized oral immunotherapy clinical trials with repeat food challenges (Q6628435) (← links)
- Sample size calculation for cluster randomization trials with a time-to-event endpoint (Q6629817) (← links)
