Evidence map›Paper›PMID 38243729›Full record

ArticleStatistics in medicine2024

Steady-state statistical properties and implementation of randomization designs with maximum tolerated imbalance restriction for two-arm equal allocation clinical trials.

Wenle Zhao, Kerstine Carter, Oleksandr Sverdlov, Annika Scheffold, Yevgen Ryeznik, Christy Cassarly, Vance W Berger

Abstract read
In one paragraph

Article in Statistics in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

7 authors.

Wenle ZhaoDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.ORCID 0000-0003-0496-9700
Kerstine CarterBiometrics and Data Sciences Department, Boehringer-Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut, USA.
Oleksandr SverdlovEarly Development Analytics, Novartis Pharmaceuticals Corporation, East Hanover, New Jersey, USA.ORCID 0000-0002-1626-2588
Annika ScheffoldBiometrics and Data Sciences Department, Boehringer-Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut, USA.
Yevgen RyeznikBioPharma Early Biometrics & Statistical Innovations, Data Science & AI, R&D BioPharmaceuticals, AstraZeneca, Gothenburg, Sweden.ORCID 0000-0003-2997-8566
Christy CassarlyDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.ORCID 0000-0002-0304-9833
Vance W BergerDivision of Cancer Prevention, National Institutes of Health, Bethesda, Maryland, USA.

Funding

Workshop to Identify Collaborative Project(s) for the NIH StrokeNet and the Japan NEtwork for Clinical Stroke Trials (NECST)U01NS087748 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Catherine R. Dillon, Jordan J. Elm · 2014 to 2026
$14.1M
Strategies to Innovate EmeRgENcy Care Clinical Trials Network (SIREN) - Data Coordinating CenterU24NS100655 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI VALERIE L DURKALSKI, Sharon Dziuba Yeatts · 2017 to 2026
$4.4M
NINDS NIH HHS U01 NS087748NINDS NIH HHS U24 NS100655
6 · The paper itself

Abstract

In recent decades, several randomization designs have been proposed in the literature as better alternatives to the traditional permuted block design (PBD), providing higher allocation randomness under the same restriction of the maximum tolerated imbalance (MTI). However, PBD remains the most frequently used method for randomizing subjects in clinical trials. This status quo may reflect an inadequate awareness and appreciation of the statistical properties of these randomization designs, and a lack of simple methods for their implementation. This manuscript presents the analytic results of statistical properties for five randomization designs with MTI restriction based on their steady-state probabilities of the treatment imbalance Markov chain and compares them to those of the PBD. A unified framework for randomization sequence generation and real-time on-demand treatment assignment is proposed for the straightforward implementation of randomization algorithms with explicit formulas of conditional allocation probabilities. Topics associated with the evaluation, selection, and implementation of randomization designs are discussed. It is concluded that for two-arm equal allocation trials, several randomization designs offer stronger protection against selection bias than the PBD does, and their implementation is not necessarily more difficult than the implementation of the PBD.

Indexed as

Models, StatisticalResearch DesignHumansProbabilityRandom AllocationSelection Biasallocation randomnessclinical trialmaximum tolerated imbalancerandomization

Identifiers

PMID38243729
PMCPMC10925840

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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.