Pages that link to "Item:Q3332138"
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The following pages link to Sample-Size Formula for the Proportional-Hazards Regression Model (Q3332138):
Displayed 26 items.
- Testing equivalence of survival before but not after end of follow-up (Q825221) (← links)
- Sample size calculation for the log-rank tests for multi-arm trials with a control (Q1031771) (← links)
- Sample size calculation for clustered survival data under subunit randomization (Q2126045) (← links)
- Sample-size calculation and reestimation for a semiparametric analysis of recurrent event data taking robust standard errors into account (Q2875758) (← links)
- Minimum Size Survival Analysis Sampling Plans for Comparing Multiple Treatment Groups to a Single Control Group (Q2921823) (← links)
- The Use of Frailty Hazard Models for Unrecognized Heterogeneity That Interacts with Treatment: Considerations of Efficiency and Power (Q3078933) (← links)
- Robust Covariate‐Adjusted Log‐Rank Statistics and Corresponding Sample Size Formula for Recurrent Events Data (Q3530090) (← links)
- Analyzing survival data in conjunction with time-dependent surrogate endpoints in clinical trials (Q4337068) (← links)
- Sample size calculation for a proportional hazards mixture cure model with nonbinary covariates (Q5036528) (← links)
- Empirical Bayes estimators in hierarchical models with mixture priors (Q5036540) (← links)
- Proportional hazards model under ranked set sampling scheme using censored data of coronary heart disease (Q5159560) (← links)
- Sample Size Requirements and Study Duration for Testing Main Effects and Interactions in Completely Randomized Factorial Designs When Time to Event is the Outcome (Q5249188) (← links)
- Heterogeneous treatment effects in stratified clinical trials with time‐to‐event endpoints (Q5348691) (← links)
- Estimation of Main Effect When Covariates Have Non-Proportional Hazards (Q5418904) (← links)
- Sample size calculation for paired survival data: a simulation method (Q5457926) (← links)
- Calculating the power or sample size for the logistic and proportional hazards models (Q5711981) (← links)
- Sample size calculations for noninferiority trials for time-to-event data using the concept of proportional time (Q5861550) (← links)
- A Simulation-Based Evaluation of the Asymptotic Power Formulas for Cox Models in Small Sample Cases (Q5876913) (← links)
- Sample size formula for general win ratio analysis (Q6055655) (← links)
- Group sequential testing for cluster randomized trials with time‐to‐event endpoint (Q6055678) (← links)
- Sample size estimation for cancer randomized trials in the presence of heterogeneous populations (Q6055721) (← links)
- Expected Precision of Estimation and Probability of Ruling Out a Hypothesis Based on a Confidence Interval (Q6064697) (← links)
- Design aspects of COVID‐19 treatment trials: Improving probability and time of favorable events (Q6068480) (← 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 determination in superiority or non-inferiority clinical trials with time-to-event data under exponential, Weibull and Gompertz distributions (Q6171850) (← links)
- Stratified modestly weighted log‐rank tests in settings with an anticipated delayed separation of survival curves (Q6183911) (← links)