Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Truncation in Survival Analysis01:09

Truncation in Survival Analysis

Truncation in survival analysis refers to the exclusion of individuals or events from the dataset based on specific criteria related to the time of the event. This exclusion can happen in two primary forms: left truncation and right truncation.
Left truncation occurs when individuals who experienced the event of interest before a certain time are not included in the study. This is often due to a "delayed entry" into the study where only those who survive until a certain entry point are observed.
Study Design in Statistics01:15

Study Design in Statistics

A study design is a set of techniques that allow a researcher to collect and analyze data from different variables defined for a specific research problem. Statistics is commonly for effective study design and more robust experiments,
Does aspirin reduce the risk of heart attacks? Is one brand of fertilizer more effective at growing roses than another? Is fatigue as dangerous to a driver as the influence of alcohol? Questions like these are answered using randomized experiments with proper...
Censoring Survival Data01:09

Censoring Survival Data

Survival analysis is a statistical method used to analyze time-to-event data, often employed in fields such as medicine, engineering, and social sciences. One of the key challenges in survival analysis is dealing with incomplete data, a phenomenon known as "censoring." Censoring occurs when the event of interest (such as death, relapse, or system failure) has not occurred for some individuals by the end of the study period or is otherwise unobservable, and it might have many different reasons...
Analysis of Population Pharmacokinetic Data01:12

Analysis of Population Pharmacokinetic Data

Analysis of population pharmacokinetic data involves studying the behavior of drugs within diverse populations to understand their pharmacokinetic parameters. Traditional pharmacokinetic methods typically involve collecting samples from a few individuals and estimating these parameters. While these methods are commonly used, they have limitations in capturing the variability in drug response among individuals or heterogeneous populations. Population pharmacokinetics is employed to address these...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Blinding01:11

Blinding

Blinding is a commonly used method of not telling participants which treatment a subject is receiving. Blinding is a critical part of a randomized control trial or RCT. It reduces the bias that affects the results. In an RCT, blinding is used in the form of a placebo. A placebo effect occurs when untreated subjects falsely believe they have received the treatment and report improved symptoms. A placebo or a dummy treatment is administered to subjects to negate the bias caused by such an effect.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A Bayesian Optimal Interval Design Considering Efficacy and Toxicity in Early Phase Basket Trials.

Pharmaceutical statistics·2026
Same author

Efficacy and safety of RApid PrednIsolone Dose reduction for acute exacerbation of Idiopathic Pulmonary Fibrosis (RAPID-IPF Trial): a study protocol for a randomised controlled trial.

BMJ open respiratory research·2026
Same author

6-mm versus 10-mm covered self-expandable metal stents and plastic stents for malignant distal biliary obstruction in resectable or borderline resectable pancreatic cancer in Japan (STARDOM, JON-2402P): study protocol for a multicenter randomized controlled trial.

Trials·2026
Same author

Multimodal intervention benefits: Responder analysis of J-MINT PRIME Kanagawa trial.

Archives of gerontology and geriatrics·2026
Same author

Optimizing chemotherapy regimens and dosing for older patients with metastatic pancreatic cancer: insights from the Tokushukai real-world data project.

BMC cancer·2026
Same author

The Verification of Co-Axiality of the Three Self-Expanding Transcatheter Aortic Valve Systems According to the Difference in Shaft Spine.

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions·2026

Related Experiment Video

Updated: Jun 12, 2026

Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index
06:55

Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index

Published on: January 8, 2020

Handing missing data using multiple imputation in hybrid control clinical trials with modified power prior.

Sunao Shimada1, Masataka Taguri1

  • 1Department of Health Data Science, Tokyo Medical University, Tokyo, Japan.

Journal of Biopharmaceutical Statistics
|June 11, 2026
PubMed
Summary

This study introduces a method for handling missing data in historical control data for hybrid clinical trials. Multiple imputation with propensity scores and power priors effectively reduces bias and improves precision, especially when historical data resembles current trial data.

Keywords:
hybrid controlmissing covariate datamodified power priormultiple imputationpropensity score matching

Related Experiment Videos

Last Updated: Jun 12, 2026

Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index
06:55

Inverse Probability of Treatment Weighting (Propensity Score) using the Military Health System Data Repository and National Death Index

Published on: January 8, 2020

Area of Science:

  • Biostatistics
  • Clinical Trial Design
  • Real-World Data Analysis

Background:

  • Randomized Controlled Trials (RCTs) are the benchmark for clinical evidence.
  • Hybrid control trials incorporating Historical Data (HD) can enhance evidence generation.
  • Real-world data (RWD) used for HD often contains missing covariate information, potentially introducing bias.

Purpose of the Study:

  • To propose and evaluate a statistical method for addressing missing covariate data in HD for hybrid control trials.
  • To assess the performance of multiple imputation combined with propensity score matching and power prior methods.
  • To investigate bias and precision under different missing data mechanisms and data similarity scenarios.

Main Methods:

  • Employed multiple imputation under the Missing At Random (MAR) assumption to handle missing covariates.
  • Utilized propensity score matching and a modified power prior approach for data analysis.
  • Conducted simulations to compare proposed methods against complete case analysis and applied the method to real clinical trial data.

Main Results:

  • Complete case analysis exhibited bias with missing at random and covariate-dependent missingness.
  • Multiple imputation yielded nearly unbiased estimates and improved precision when HD was similar to current trial data (MAR assumption).
  • The method dynamically borrowed information from HD based on outcome similarity, enhancing accuracy and power while controlling Type I error.

Conclusions:

  • The proposed method effectively handles missing covariate data in HD for hybrid control trials.
  • Multiple imputation offers a robust solution, outperforming complete case analysis.
  • The approach demonstrates practical utility and potential for improving hybrid trial designs using RWD.