Sample size re-estimation without unblinding for normally distributed outcomes with unknown variance

DOI10.1080/03610929208830947zbMath0775.62298OpenAlexW2146671770WikidataQ56778031 ScholiaQ56778031MaRDI QIDQ4202692

A. Lawrence Gould, Weichung Joseph Shih

Publication date: 4 October 1993

Published in: Communications in Statistics - Theory and Methods (Search for Journal in Brave)

Full work available at URL: https://doi.org/10.1080/03610929208830947

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10)

Related Items (24)

Bayesian blinded sample size re-estimation ⋮ Distribution theory following blinded and unblinded sample size re-estimation under parametric models ⋮ Semi-blinded design in clinical trials ⋮ Generalized Likelihood Ratio Statistics and Uncertainty Adjustments in Efficient Adaptive Design of Clinical Trials ⋮ Blinded versus unblinded estimation of a correlation coefficient to inform interim design adaptations ⋮ Variance Estimation in Clinical Studies with Interim Sample Size Reestimation ⋮ Blinded sample size re-estimation with unequal variances and center effects in clinical trials ⋮ Issues in blinded sample size re-estimation ⋮ Sample size determination and re‐estimation for matched pair designs with multiple binary endpoints ⋮ Practical Methods for Bounding Type I Error Rate with an Internal Pilot Design ⋮ Modification of Sample Size in Group Sequential Clinical Trials ⋮ An Improved Double Sampling Procedure Based on the Variance ⋮ Blinded sample size recalculation in multicentre trials with normally distributed outcome ⋮ Internal pilots for observational studies ⋮ Sequential Methods in Multi-Arm Clinical Trials ⋮ Blinded and unblinded sample size reestimation in crossover trials balanced for period ⋮ Controlling Test Size While Gaining the Benefits of an Internal Pilot Design ⋮ Sample-Size Redetermination for Repeated Measures Studies ⋮ Sequential Conditional Probability Ratio Tests for Normalized Test Statistic on Information Time ⋮ Optimal sampling in retrospective logistic regression via two-stage method ⋮ Basic concepts of group sequential and adaptive group sequential test procedures ⋮ EM Estimation for Finite Mixture Models with Known Mixture Component Size ⋮ THE ATTRACTIVENESS OF THE CONCEPT OF A PROSPECTIVELY DESIGNED TWO-STAGE CLINICAL TRIAL ⋮ Sample-size calculation and reestimation for a semiparametric analysis of recurrent event data taking robust standard errors into account

Cites Work

• Some Methods for Studying the Mixture of Two Normal (Lognormal) Distributions
• Inference and missing data
• A Two-Sample Test for a Linear Hypothesis Whose Power is Independent of the Variance

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