Background: Incomplete data analysis continues to be a major issue for non-inferiority clinical trials. Due to the steadily increasing use of non-inferiority study design, we believe this topic deserves an immediate attention.

Methods: We evaluated the performance of various strategies, including complete case analysis and various imputations techniques for handling incomplete non-inferiority clinical trials when outcome of interest is difference between binomial proportions. Non-inferiority of a new treatment was determined using a fixed margin approach with 95-95% confidence interval method. The methods used to construct the confidence intervals were compared as well and included: Wald, Farrington-Manning and Newcombe methods.

Results: We found that worst-case and best-case scenario imputation methods should not be used for analysis of incomplete data in non-inferiority trial design, since such methods seriously inflate type-I error rates and produce biased estimates. In addition, we report conditions under which complete case analysis is an acceptable strategy for missing at random missingness mechanism. Importantly, we show how two-stage multiple imputation could be successfully applied for incomplete data that follow missing not at random patterns, and thus result in controlled type-I error rates and unbiased estimates.

Conclusion: This thorough simulation study provides a road map for the analysis of incomplete data in non-inferiority clinical trials for different types of missingness. We believe that the results reported in this paper could serve practitioners who encounter missing data problems in their non-inferiority clinical trials.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226649PMC
http://dx.doi.org/10.1016/j.conctc.2020.100567DOI Listing

Publication Analysis

Top Keywords

incomplete data
20
non-inferiority clinical
20
clinical trials
20
data analysis
8
non-inferiority
8
difference binomial
8
binomial proportions
8
complete case
8
case analysis
8
analysis incomplete
8

Similar Publications

Biomedical datasets are the mainstays of computational biology and health informatics projects, and can be found on multiple data platforms online or obtained from wet-lab biologists and physicians. The quality and the trustworthiness of these datasets, however, can sometimes be poor, producing bad results in turn, which can harm patients and data subjects. To address this problem, policy-makers, researchers, and consortia have proposed diverse regulations, guidelines, and scores to assess the quality and increase the reliability of datasets.

View Article and Find Full Text PDF

The influence of sintering of osteoporotic vertebral fractures on the sagittal lumbar profile and degenerative changes.

J Orthop Surg Res

January 2025

Department of Orthopaedic and Trauma Surgery, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine-University, Düsseldorf, Germany.

Background: Osteoporosis, a skeletal disorder affecting nearly 20% of the global population, poses a significant health concern, with osteoporotic vertebral body fractures (VBF) representing a common clinical manifestation. The impact of osteoporotic sintering fractures in the thoracolumbar spine on the sagittal lumbar profile is incompletely understood and may lead to the onset of clinical symptoms in previously asymptomatic patients.

Methods: This retrospective single-center study analyzed data from patients presenting with osteoporotic spine fractures between 2017 and 2022.

View Article and Find Full Text PDF

Predicting cell morphological responses to perturbations using generative modeling.

Nat Commun

January 2025

Department of Computational Health, Institute of Computational Biology, Helmholtz Zentrum München, Munich, Germany.

Advancements in high-throughput screenings enable the exploration of rich phenotypic readouts through high-content microscopy, expediting the development of phenotype-based drug discovery. However, analyzing large and complex high-content imaging screenings remains challenging due to incomplete sampling of perturbations and the presence of technical variations between experiments. To tackle these shortcomings, we present IMage Perturbation Autoencoder (IMPA), a generative style-transfer model predicting morphological changes of perturbations across genetic and chemical interventions.

View Article and Find Full Text PDF

Purpose: This study aimed to determine complete toxicity reporting (CTR), and the use of subjective toxicity-minimizing language (TML) among phase III oncology trials.

Methods: Two-arm superiority-design phase III oncology trials published from 2002 to 2020 were reviewed for toxicity data. CTR was defined as reporting total adverse events (TAEs), total serious adverse events (SAEs), total deaths, and study therapy discontinuations because of toxicity.

View Article and Find Full Text PDF

Background: Adults with intellectual or developmental disability (IDD) are at higher risk for incomplete cancer staging.

Aim: To compare unknown stage data between those with and without IDD.

Materials And Methods: We used the Ontario Cancer Registry linked to administrative health data between 2007 and 2019.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!