Evidence map›Paper›PMID 42751965›Full record

ArticleStatistics in medicine2026

Comparing Missing Data Strategies for Generalized Pairwise Comparisons in Randomized Clinical Trials: A Simulation Study.

Ruben P A van Eijk, Ying Lu

Abstract readComparative Study
In one paragraph

Article in Statistics in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Ruben P A van EijkDepartment of Biomedical Data Science and Centre for Innovative Study Designs, School of Medicine, Stanford University, Stanford, California, USA.ORCID https://orcid.org/0000-0002-7132-5967
Ying LuDepartment of Biomedical Data Science and Centre for Innovative Study Designs, School of Medicine, Stanford University, Stanford, California, USA.ORCID https://orcid.org/0000-0002-7698-8962

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek VENI 09150162210036U.S. Department of Defense AL230152
6 · The paper itself

Abstract

Generalized pairwise comparisons are increasingly being used in randomized clinical trials. This study evaluates how missing data strategies impact the operating characteristics of endpoints combining overall survival and a longitudinal outcome. A simulation study was conducted to evaluate the impact of censoring and missing longitudinal data on the Type I error, power, and bias of a hierarchical composite endpoint. Seven missing data strategies were identified from the literature, including assigning ties to missing patient pairs, comparing patients at their last common visit, and applying multiple imputation. Conditional longitudinal and survival data were generated based on the natural history of amyotrophic lateral sclerosis. Simulation scenarios varied in censoring rates, extent of missing longitudinal data, differential attrition between treatment arms, and the dependency of missingness on disease severity. All methods were unbiased and maintained nominal Type I error when censoring and missingness were balanced across treatment arms. Under imbalance, however, Type I error increased-reaching up to 0.378 for some strategies. The last common visit strategy was the only approach that consistently preserved nominal error rates (0.025 ± 0.002). Regarding statistical power, all methods exhibited a loss of precision and increased bias under the alternative hypothesis as missingness increased. Multiple imputation partially recovered power and reduced bias but inflated the Type I error rate in scenarios with differential attrition. As generalized pairwise comparisons are increasingly used in pivotal clinical trials-and therefore in regulatory contexts-our findings provide practical guidance for selecting a robust primary analysis strategy and minimizing bias arising from incomplete data.

Indexed as

Randomized Controlled Trials as TopicAmyotrophic Lateral SclerosisBiasComputer SimulationData Interpretation, StatisticalEndpoint DeterminationHumansLongitudinal StudiesModels, StatisticalSurvival Analysisamyotrophic lateral sclerosisclinical trialscombined assessment of function and survivalgeneralized pairwise comparisonshierarchical endpointwin statistics

Identifiers

PMID42751965
PMCPMC13584238

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.