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Clinical trials : a methodologic perspective
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ISBN: 0471163937 9780471163930 Year: 1997 Volume: 1346 Publisher: New York: Wiley,

Clinical trials : a methodologic perspective
Author:
ISBN: 9780471727811 0471727814 Year: 2005 Publisher: Hoboken: Wiley,

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Abstract

Learn rigorous statistical methods to ensure valid clinical trialsThis Second Edition of the critically hailed Clinical Trials builds on the text's reputation as a straightforward and authoritative presentation of statistical methods for clinical trials. Readers are introduced to the fundamentals of design for various types of clinical trials and then skillfully guided through the complete process of planning the experiment, assembling a study cohort, assessing data, and reporting results. Throughout the process, the author alerts readers to problems that may arise during the course of


Book
Clinical trials : a methodologic perspective
Author:
ISBN: 9781118959206 9781118959220 1118959205 Year: 2017 Publisher: Hoboken: Wiley,

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This Third Edition builds on the text's reputation as a straightforward, detailed, and authoritative presentation of quantitative methods for clinical trials. Readers will encounter the principles of design for various types of clinical trials, and are then skillfully guided through the complete process of planning the experiment, assembling a study cohort, assessing data, and reporting results. Throughout the process, the author alerts readers to problems that may arise during the course of the trial and provides common sense solutions.All stages of therapeutic development are discussed in detail, and the methods are not restricted to a single clinical application area. The author bases current revisions and updates on his own experience, classroom instruction, and feedback from teachers and medical and statistical professionals involved in clinical trials. The Third Edition greatly expands its coverage, ranging from statistical principles to new and provocative topics, including alternative medicine and ethics, middle development comparative studies, and adaptive designs.At the same time, it offers more pragmatic advice for issues such as selecting outcomes, sample size, analysis, reporting, and handling allegations of misconduct. Readers familiar with the First and Second Editions will discover revamped exercise sets, an updated and extensive reference section, new material on endpoints and the developmental pipeline, among others, and revisions of numerous sections.In addition, this book : - Features accessible and broad coverage of statistical design methods—the crucial building blocks of clinical trials and medical research—now complete with new chapters on overall development, middle development, comparative studies, and adaptive designs ; - Teaches readers to design clinical trials that produce valid qualitative results backed by rigorous statistical methods ; - Contains an introduction and summary in each chapter to reinforce key points ; - Includes discussion questions to stimulate critical thinking and help readers understand how they can apply their newfound knowledge ; - Provides extensive references to direct readers to the most recent literature ; - Includes numerous new or revised exercises throughout.


Digital
Clinical trials : a methodologic perspective
Author:
ISBN: 9781118959206 9781118959220 Year: 2017 Publisher: Hoboken, N.J. John Wiley & Sons

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Clinical trials : a methodologic perspective
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ISBN: 9780471727811 Year: 2005 Publisher: Hoboken, N.J. Wiley

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Book
Clinical trials : a methodologic perspective
Author:
ISBN: 9781394195664 Year: 2024 Publisher: Hoboken, New Jersey : Wiley,

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"This Fourth Edition builds on the text's reputation as a straightforward, detailed, and authoritative presentation of quantitative methods for clinical trials. Readers will encounter principles of design for various types of clinical trials and are then skillfully guided through the complete process of planning the experiment, assembling a study cohort, assessing data, and reporting results. Throughout the process, the author alerts readers to problems that may arise during the course of a trial and provides common sense solutions. The Fourth Edition greatly expands its coverage, ranging from statistical principles to new and provocative topics, including four new chapters on generalizing results, operating characteristics, trial issues during the COVID-19 pandemic, and clinical trials using so-called "real world" data. Existing topics have been updated and expanded such as alternative medicine, ethics, middle development, comparative studies, and adaptive designs. Readers familiar with prior editions will discover revamped exercise sets; an updated and extensive reference section; new material on endpoints and the developmental pipeline, among others; and revisions of numerous sections."--


Book
Principles and practice of clinical trials
Authors: ---
ISBN: 3319526367 Year: 2022 Publisher: Cham, Switzerland : Springer,

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This is a comprehensive major reference work for our SpringerReference program covering clinical trials. Although the core of the Work will focus on the design, analysis, and interpretation of scientific data from clinical trials, a broad spectrum of clinical trial application areas will be covered in detail. This is an important time to develop such a Work, as drug safety and efficacy emphasizes the Clinical Trials process. Because of an immense and growing international disease burden, pharmaceutical and biotechnology companies continue to develop new drugs. Clinical trials have also become extremely globalized in the past 15 years, with over 225,000 international trials ongoing at this point in time.


Digital
Principles and Practice of Clinical Trials
Authors: ---
ISBN: 9783319526775 Year: 2020 Publisher: Cham Springer International Publishing

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This is a comprehensive major reference work for our SpringerReference program covering clinical trials. Although the core of the Work will focus on the analysis and interpretation of scientific data gleaned from the trial process, a broad spectrum of clinical trial principles and practice areas will be covered in detail. This is an important time to develop such a Work, as drug safety and efficacy cannot be guaranteed and regulated without the Clinical Trials process. Because of an immense and continuing to grow international disease burden, pharmaceutical and biotechnology companies continue to develop new drugs. Clinical trials have also become extremely globalized in the past 15 years, with over 225,000 international trials ongoing at this point in time. Principles in Practice of Clinical Trials is truly an interdisciplinary that will be divided into the following areas: 1) Clinical Trials Basic Perspectives 2) Regulation and Oversight 3) Basic Trial Designs 4) Advanced Trial Designs 5) Analysis 6) Trial Publication 7) Topics Related Specific Populations and Legal Aspects of Clinical Trials The Work is designed to be comprised of 175 chapters and approximately 2500 pages. The Work will be oriented like many of our SpringerReference Handbooks, presenting detailed and comprehensive expository chapters on broad subjects. The Editors are major figures in the field of clinical trials, and both have written textbooks on the topic. There will also be a slate of 7-8 renowned associate editors that will edit individual sections of the Reference.


Multi
Principles and Practice of Clinical Trials
Authors: ---
ISBN: 9783319526362 9783319526355 Year: 2022 Publisher: Cham Springer International Publishing

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Volume 1 Part I Perspectives on Clinical Trials – Part II Conduct and Management – Part III Regulation and Oversight – Volume 2 Part IV Bias Control and Precision – Part V Basics of Trial Design – Part VI Advanced Topics in Trial Design – Volume 3 Part VIII Analysis – Part VIII Publication and Related Issues – Part IX Special Topics


Book
Principles and Practice of Clinical Trials
Authors: ---
ISBN: 3319526774 Year: 2020 Publisher: Cham : Springer International Publishing : Imprint: Springer,

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This is a comprehensive major reference work for our SpringerReference program covering clinical trials. Although the core of the Work will focus on the analysis and interpretation of scientific data gleaned from the trial process, a broad spectrum of clinical trial principles and practice areas will be covered in detail. This is an important time to develop such a Work, as drug safety and efficacy cannot be guaranteed and regulated without the Clinical Trials process. Because of an immense and continuing to grow international disease burden, pharmaceutical and biotechnology companies continue to develop new drugs. Clinical trials have also become extremely globalized in the past 15 years, with over 225,000 international trials ongoing at this point in time. Principles in Practice of Clinical Trials is truly an interdisciplinary that will be divided into the following areas: 1) Clinical Trials Basic Perspectives 2) Regulation and Oversight 3) Basic Trial Designs 4) Advanced Trial Designs 5) Analysis 6) Trial Publication 7) Topics Related Specific Populations and Legal Aspects of Clinical Trials The Work is designed to be comprised of 175 chapters and approximately 2500 pages. The Work will be oriented like many of our SpringerReference Handbooks, presenting detailed and comprehensive expository chapters on broad subjects. The Editors are major figures in the field of clinical trials, and both have written textbooks on the topic. There will also be a slate of 7-8 renowned associate editors that will edit individual sections of the Reference.

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