Literature DB >> 26868369

Simulation of various randomization strategies for a clinical trial in sickle cell disease.

William J Meurer1, Jason T Connor2,3, Jeffrey Glassberg4.   

Abstract

OBJECTIVE: To use numerical simulation to evaluate various randomization strategies for a clinical trial in sickle cell disease (SCD).
METHODS: The Inhaled Mometasone to Promote Reduction in Vaso-occlusive Events trial* is a randomized, controlled, feasibility study of inhaled mometasone for individuals with SCD who do not have asthma. The target sample size is 45 patients and one goal is to limit imbalance with respect to two important covariates (1) hydroxyurea use and (2) historical emergency department (ED) utilization. We compared three methods of patient allocation (simple randomization, block randomization, and biased-coin adaptive randomization) using numerical simulation (10 000 trials). The primary outcome measure was the proportion of simulated trials with numerically apparent differences in the two covariates: hydroxyurea use (binary) and ED utilization (three-level ordinal).
RESULTS: Overall, only 1.6% of simulated trials had any covariate comparison with P < 0.3 across groups for simple randomization, and 0% for both the block and adaptive randomization. In trials where the total sample size was 45 patients, the block randomization strategy achieved the greatest balance because participants were deterministically assigned to the treatment arm that balanced covariates. The adaptive strategy achieved similar results without deterministic treatment assignments even when trials included only 45 patients. DISCUSSION: Adaptive clinical trial designs have potential to mitigate some of the challenges that have hampered SCD trials. In small exploratory trials, even non-statistically significant differences in important covariates can threaten interpretability and external validity.
CONCLUSION: Adaptive randomization performed similarly to block randomization and offers advantages including better allocation concealment and less ability for investigators to predict the next assignment.

Entities:  

Keywords:  Adaptive clinical trials; Bayesian statistics; Clinical trials; Sickle cell disease

Mesh:

Substances:

Year:  2016        PMID: 26868369      PMCID: PMC5012429          DOI: 10.1080/10245332.2015.1101966

Source DB:  PubMed          Journal:  Hematology        ISSN: 1024-5332            Impact factor:   2.269


  16 in total

1.  Painful episodes in children with sickle cell disease and asthma are temporally associated with respiratory symptoms.

Authors:  Jeffrey Glassberg; John F Spivey; Robert Strunk; Sara Boslaugh; Michael R DeBaun
Journal:  J Pediatr Hematol Oncol       Date:  2006-08       Impact factor: 1.289

2.  Testing for baseline balance in clinical trials.

Authors:  S Senn
Journal:  Stat Med       Date:  1994-09-15       Impact factor: 2.373

3.  The burden of emergency department use for sickle-cell disease: an analysis of the national emergency department sample database.

Authors:  Sophie Lanzkron; C Patrick Carroll; Carlton Haywood
Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

4.  Recurrent, severe wheezing is associated with morbidity and mortality in adults with sickle cell disease.

Authors:  Robyn T Cohen; Anusha Madadi; Morey A Blinder; Michael R DeBaun; Robert C Strunk; Joshua J Field
Journal:  Am J Hematol       Date:  2011-08-02       Impact factor: 10.047

5.  Risk factors for increased ED utilization in a multinational cohort of children with sickle cell disease.

Authors:  Jeffrey A Glassberg; Jason Wang; Robyn Cohen; Lynne D Richardson; Michael R DeBaun
Journal:  Acad Emerg Med       Date:  2012-06       Impact factor: 3.451

6.  Clinical trial implementation and recruitment: lessons learned from the early closure of a randomized clinical trial.

Authors:  Marlene H Peters-Lawrence; Margaret C Bell; Lewis L Hsu; Ifeyinwa Osunkwo; Phillip Seaman; Miren Blackwood; Edouard Guillaume; Rita Bellevue; Lakshmanan Krishnamurti; Wally R Smith; Carlton D Dampier; Caterina P Minniti
Journal:  Contemp Clin Trials       Date:  2011-12-02       Impact factor: 2.226

7.  Wheezing and asthma are independent risk factors for increased sickle cell disease morbidity.

Authors:  Jeffrey A Glassberg; Annie Chow; Juan Wisnivesky; Ronald Hoffman; Michael R Debaun; Lynne D Richardson
Journal:  Br J Haematol       Date:  2012-09-12       Impact factor: 6.998

8.  Subgroup analysis, covariate adjustment and baseline comparisons in clinical trial reporting: current practice and problems.

Authors:  Stuart J Pocock; Susan E Assmann; Laura E Enos; Linda E Kasten
Journal:  Stat Med       Date:  2002-10-15       Impact factor: 2.373

Review 9.  Sickle cell pain: a critical reappraisal.

Authors:  Samir K Ballas; Kalpna Gupta; Patricia Adams-Graves
Journal:  Blood       Date:  2012-08-24       Impact factor: 22.113

10.  Dynamic balanced randomization for clinical trials.

Authors:  D F Signorini; O Leung; R J Simes; E Beller; V J Gebski; T Callaghan
Journal:  Stat Med       Date:  1993-12-30       Impact factor: 2.373

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  1 in total

1.  Inhaled steroids reduce pain and sVCAM levels in individuals with sickle cell disease: A triple-blind, randomized trial.

Authors:  Jeffrey Glassberg; Caterina Minnitti; Caroline Cromwell; Lawrence Cytryn; Thomas Kraus; Gwen S Skloot; Jason T Connor; Adeeb H Rahman; William J Meurer
Journal:  Am J Hematol       Date:  2017-06-05       Impact factor: 10.047

  1 in total

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