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Understanding an impact of patient enrollment pattern on predictability of central (unstratified) randomization in a multi-center clinical trial.
Krisam, Johannes; Ryeznik, Yevgen; Carter, Kerstine; Kuznetsova, Olga; Sverdlov, Oleksandr.
Afiliación
  • Krisam J; Global Biostatistics and Data Sciences, Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, Germany.
  • Ryeznik Y; Department of Pharmacy, Uppsala University, Uppsala, Sweden.
  • Carter K; Global Biostatistics and Data Sciences, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, Connecticut, USA.
  • Kuznetsova O; Merck & Co., Inc., Rahway, New Jersey, USA.
  • Sverdlov O; Novartis Pharmaceuticals Corporation, East Hanover, New Jersey, USA.
Stat Med ; 43(17): 3313-3325, 2024 Jul 30.
Article en En | MEDLINE | ID: mdl-38831520
ABSTRACT
In a multi-center randomized controlled trial (RCT) with competitive recruitment, eligible patients are enrolled sequentially by different study centers and are randomized to treatment groups using the chosen randomization method. Given the stochastic nature of the recruitment process, some centers may enroll more patients than others, and in some instances, a center may enroll multiple patients in a row, for example, on a given day. If the study is open-label, the investigators might be able to make intelligent guesses on upcoming treatment assignments in the randomization sequence, even if the trial is centrally randomized and not stratified by center. In this paper, we use enrollment data inspired by a real multi-center RCT to quantify the susceptibility of two restricted randomization procedures, the permuted block design and the big stick design, to selection bias under the convergence strategy of Blackwell and Hodges (1957) applied at the center level. We provide simulation evidence that the expected proportion of correct guesses may be greater than 50% (i.e., an increased risk of selection bias) and depends on the chosen randomization method and the number of study patients recruited by a given center that takes consecutive positions on the central allocation schedule. We propose some strategies for ensuring stronger encryption of the randomization sequence to mitigate the risk of selection bias.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ensayos Clínicos Controlados Aleatorios como Asunto / Estudios Multicéntricos como Asunto / Selección de Paciente Límite: Humans Idioma: En Revista: Stat Med Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ensayos Clínicos Controlados Aleatorios como Asunto / Estudios Multicéntricos como Asunto / Selección de Paciente Límite: Humans Idioma: En Revista: Stat Med Año: 2024 Tipo del documento: Article País de afiliación: Alemania