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showing 10 items of 2844 documents

Marginal hazard ratio estimates in joint frailty models for heart failure trials

2019

Abstract This work is motivated by clinical trials in chronic heart failure disease, where treatment has effects both on morbidity (assessed as recurrent non‐fatal hospitalisations) and on mortality (assessed as cardiovascular death, CV death). Recently, a joint frailty proportional hazards model has been proposed for these kind of efficacy outcomes to account for a potential association between the risk rates for hospital admissions and CV death. However, more often clinical trial results are presented by treatment effect estimates that have been derived from marginal proportional hazards models, that is, a Cox model for mortality and an Andersen–Gill model for recurrent hospitalisations. …

Statistics and ProbabilityBiometryleast false parameterDiseasejoint frailty modelRisk AssessmentStudy durationCardiovascular deathunexplained heterogeneitymedicineHumansTreatment effectComplex Regression ModelsProportional Hazards ModelsHeart FailureClinical Trials as TopicProportional hazards modelbusiness.industryheart failure trialsHazard ratioGeneral Medicinemedicine.diseaseClinical trialrecurrent eventsHeart failureAsymptomatic DiseasesStatistics Probability and UncertaintybusinessDemographyResearch PaperBiometrical Journal. Biometrische Zeitschrift
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Power of the Wilcoxon–Mann–Whitney test for non‐inferiority in the presence of death‐censored observations

2017

In clinical trials with patients in a critical state, death may preclude measurement of a quantitative endpoint of interest, and even early measurements, for example for intention-to-treat analysis, may not be available. For example, a non-negligible proportion of patients with acute pulmonary embolism will die before 30 day measurements on the efficacy of thrombolysis can be obtained. As excluding such patients may introduce bias, alternative analyses, and corresponding means for sample size calculation are needed. We specifically consider power analysis in a randomized clinical trial setting in which the goal is to demonstrate noninferiority of a new treatment as compared to a reference t…

Statistics and ProbabilityClinical Trials as TopicBiometryEndpoint Determinationbusiness.industryNonparametric statisticsGeneral Medicinemedicine.diseaseOutcome (probability)Pulmonary embolismlaw.inventionDeathClinical trialRandomized controlled trialSample size determinationlawCensoring (clinical trials)StatisticsMann–Whitney U testHumansMedicineStatistics Probability and UncertaintyPulmonary EmbolismbusinessBiometrical Journal
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Opportunities and challenges of combined effect measures based on prioritized outcomes

2013

Many authors have proposed different approaches to combine multiple endpoints in a univariate outcome measure in the literature. In case of binary or time-to-event variables, composite endpoints, which combine several event types within a single event or time-to-first-event analysis are often used to assess the overall treatment effect. A main drawback of this approach is that the interpretation of the composite effect can be difficult as a negative effect in one component can be masked by a positive effect in another. Recently, some authors proposed more general approaches based on a priority ranking of outcomes, which moreover allow to combine outcome variables of different scale levels. …

Statistics and ProbabilityClinical Trials as TopicEpidemiologyUnivariatecomputer.software_genreOutcome (game theory)Treatment OutcomeRankingScale (social sciences)Component (UML)Outcome Assessment Health CareMultiple comparisons problemHumansComputer SimulationData miningcomputerProportional Hazards ModelsMathematicsStatistical hypothesis testingEvent (probability theory)Statistics in Medicine
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Sample size planning for survival prediction with focus on high-dimensional data

2011

Sample size planning should reflect the primary objective of a trial. If the primary objective is prediction, the sample size determination should focus on prediction accuracy instead of power. We present formulas for the determination of training set sample size for survival prediction. Sample size is chosen to control the difference between optimal and expected prediction error. Prediction is carried out by Cox proportional hazards models. The general approach considers censoring as well as low-dimensional and high-dimensional explanatory variables. For dimension reduction in the high-dimensional setting, a variable selection step is inserted. If not all informative variables are included…

Statistics and ProbabilityClustering high-dimensional dataClinical Trials as TopicLung NeoplasmsModels StatisticalKaplan-Meier EstimateEpidemiologyProportional hazards modelDimensionality reductionGene ExpressionFeature selectionKaplan-Meier EstimateBiostatisticsPrognosisBrier scoreSample size determinationCarcinoma Non-Small-Cell LungSample SizeCensoring (clinical trials)StatisticsHumansProportional Hazards ModelsMathematicsStatistics in Medicine
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Assessing covariate imbalance in meta-analysis studies.

2010

The main goal of meta-analysis is to combine data across studies or data sets to obtain summary estimates. In this paper, the novelty is to propose a statistical tool to assess a possible covariate imbalance in baseline variables to investigate similarity of trials. We conducted the detection of the covariate imbalance, first, through some graphical comparison of the empirical cumulative distribution functions or ECDFs, which are built by putting together arms or trials according to some risk factor, and second, through some non-parametric tests such as the Kolmogorov–Smirnov and the Anderson–Darling tests. To overcome the huge presence of ties, we conducted the statistical tests on perturbe…

Statistics and ProbabilityMaleperturbationEpidemiologyComputer sciencePoolingHypercholesterolemiaAlpha interferonMeta-Analysis as TopicCovariateStatisticsEconometricsHumansSettore SECS-S/05 - Statistica SocialeECDFnon-parametric testStatistical hypothesis testingRandomized Controlled Trials as TopicCumulative distribution functionNonparametric statisticsNoveltyInterferon-alphacombinabilityHepatitis C ChronicMeta-analysisData Interpretation StatisticalFemaleHydroxymethylglutaryl-CoA Reductase InhibitorsStatistics in medicine
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Adaptive designs with correlated test statistics

2009

In clinical trials, the collected observations such as clustered data or repeated measurements are often correlated. As a consequence, test statistics in a multistage design are correlated. Adaptive designs were originally developed for independent test statistics. We present a general framework for two-stage adaptive designs with correlated test statistics. We show that the significance level for the Bauer-Köhne design is inflated for positively correlated test statistics from a bivariate normal distribution. The decision boundary for the second stage can be modified so that type one error is controlled. This general concept is expandable to other adaptive designs. In order to use these de…

Statistics and ProbabilityOptimal designClinical Trials as TopicBiometryModels StatisticalEpidemiologyCovariance matrixMultivariate normal distributionWald testGeneralized linear mixed modelExact testSample size determinationStatisticsLinear ModelsHumansMathematicsStatistical hypothesis testingStatistics in Medicine
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Powerful short-cuts for multiple testing procedures with special reference to gatekeeping strategies.

2007

In this paper we present a general testing principle for a class of multiple testing problems based on weighted hypotheses. Under moderate conditions, this principle leads to powerful consonant multiple testing procedures. Furthermore, short-cut versions can be derived, which simplify substantially the implementation and interpretation of the related test procedures. It is shown that many well-known multiple test procedures turn out to be special cases of this general principle. Important examples include gatekeeping procedures, which are often applied in clinical trials when primary and secondary objectives are investigated, and multiple test procedures based on hypotheses which are comple…

Statistics and ProbabilityResearch designClass (computer programming)Clinical Trials as TopicGatekeepingInterpretation (logic)Models StatisticalEpidemiologybusiness.industryTest proceduresMachine learningcomputer.software_genreGatekeepingEuropesymbols.namesakeBonferroni correctionResearch DesignMultiple comparisons problemsymbolsHumansArtificial intelligencebusinessAlgorithmcomputerMathematicsStatistics in medicine
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Performance of adaptive sample size adjustment with respect to stopping criteria and time of interim analysis

2006

The benefit of adjusting the sample size in clinical trials on the basis of treatment effects observed in interim analysis has been the subject of several recent papers. Different conclusions were drawn about the usefulness of this approach for gaining power or saving sample size, because of differences in trial design and setting. We examined the benefit of sample size adjustment in relation to trial design parameters such as 'time of interim analysis' and 'choice of stopping criteria'. We compared the adaptive weighted inverse normal method with classical group sequential methods for the most common and for optimal stopping criteria in early, half-time and late interim analyses. We found …

Statistics and ProbabilityResearch designClinical Trials as TopicEpidemiologyComputer scienceInterim analysisClinical trialNormal-inverse Gaussian distributionSequential methodResearch DesignSample size determinationSample SizeInterimStatisticsEconometricsHumansOptimal stoppingStatistics in Medicine
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Inferential tools in penalized logistic regression for small and sparse data: A comparative study.

2016

This paper focuses on inferential tools in the logistic regression model fitted by the Firth penalized likelihood. In this context, the Likelihood Ratio statistic is often reported to be the preferred choice as compared to the ‘traditional’ Wald statistic. In this work, we consider and discuss a wider range of test statistics, including the robust Wald, the Score, and the recently proposed Gradient statistic. We compare all these asymptotically equivalent statistics in terms of interval estimation and hypothesis testing via simulation experiments and analyses of two real datasets. We find out that the Likelihood Ratio statistic does not appear the best inferential device in the Firth penal…

Statistics and ProbabilityScore testPRESS statisticEpidemiologyStatistics as TopicScoreWald testLogistic regression01 natural sciences010104 statistics & probability03 medical and health sciences0302 clinical medicineHealth Information ManagementStatisticsEconometricsHumans030212 general & internal medicine0101 mathematicsStatisticMathematicsLikelihood FunctionsModels StatisticalLogistic regression firth penalized likelihood sandwich formula score statistic gradient statisticLogistic ModelsLikelihood-ratio testData Interpretation StatisticalSample SizeAncillary statisticSettore SECS-S/01 - StatisticaStatistical methods in medical research
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Test and power considerations for multiple endpoint analyses using sequentially rejective graphical procedures

2009

A variety of powerful test procedures are available for the analysis of clinical trials addressing multiple objectives, such as comparing several treatments with a control, assessing the benefit of a new drug for more than one endpoint, etc. However, some of these procedures have reached a level of complexity that makes it difficult to communicate the underlying test strategies to clinical teams. Graphical approaches have been proposed instead that facilitate the derivation and communication of Bonferroni-based closed test procedures. In this paper we give a coherent description of the methodology and illustrate it with a real clinical trial example. We further discuss suitable power measur…

Statistics and ProbabilityTest strategyEndpoint DeterminationEpidemiologyComputer scienceControl (management)Analysis of clinical trialsMachine learningcomputer.software_genresymbols.namesakeDrug TherapyComputer GraphicsConfidence IntervalsHumansMulticenter Studies as TopicRandomized Controlled Trials as Topicbusiness.industryVariety (cybernetics)Test (assessment)Clinical trialBonferroni correctionClinical Trials Phase III as TopicData Interpretation StatisticalMultiple comparisons problemsymbolsArtificial intelligencebusinessAlgorithmcomputerStatistics in Medicine
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