Title
ClinicalTrials: Design, Conduct and Analysis (Monographs in Epidemiology and Biostatistics),New
Delivery time: 8-12 business days (International)
First published in 1986, this landmark text is the definitive guide to clinical trials, written by one of the leading experts in the field. This fullyupdated second edition continues to be the most authoritative reference text on randomized clinical trials. It contains a wealth of practical information on the design, conduct, and analysis of both single center and multicenter trials. No other book on clinical trials offers as much detail on such issues as sample size calculation, stratification and randomization, data systems design, development of consent forms, publication policies, preparation of funding requests, and reporting procedures.While the basics of design, conduct, and analysis of clinical trials remain the same, there have been significant changes since the first edition of Clinical Trials was published two decades ago. In this new edition, the author discusses the refinements and improvements made to methods and procedures, changes in the policies and guidelines underlying trials, as well as requirements for registration of trials. He also discusses current practices for data sharing, for gender representation, for treatment effects monitoring, and for ethical standards of clinical trials. The importance of the randomized controlled trial has grown significantly over time and they are now the cornerstone of all evidencebased medicine. Still rich in tables, checklists, charts, and other resources for the trialist, the second edition of Clinical Trials is an indispensable reference for clinicians, biostaticians, epidemiologists, and anyone involved in the design and implementation of a clinical trial.
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We ship your order within 2–3 business days for USA deliveries and 5–8 business days for international shipments. Once your package has been dispatched from our warehouse, you'll receive an email confirmation with a tracking number, allowing you to track the status of your delivery.
Returns
To facilitate a smooth return process, a Return Authorization (RA) Number is required for all returns. Returns without a valid RA number will be declined and may incur additional fees. You can request an RA number within 15 days of the original delivery date. For more details, please refer to our Return & Refund Policy page.
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Warranty
We provide a 2-year limited warranty, from the date of purchase for all our products.
If you believe you have received a defective product, or are experiencing any problems with your product, please contact us.
This warranty strictly does not cover damages that arose from negligence, misuse, wear and tear, or not in accordance with product instructions (dropping the product, etc.).
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Frequently Asked Questions
- Q: What is the primary focus of 'ClinicalTrials: Design, Conduct and Analysis'? A: This book serves as a comprehensive guide to the design, conduct, and analysis of clinical trials, emphasizing randomized clinical trials and their role in evidence-based medicine.
- Q: Who is the author of this book? A: The book is authored by Curtis L. Meinert, PhD, a recognized expert in the field of clinical trials.
- Q: What edition of the book is available? A: The available edition is the second edition, which was published on March 27, 2012.
- Q: How many pages does this book contain? A: The book contains 720 pages filled with detailed information and resources related to clinical trials.
- Q: What topics are covered in the book? A: The book covers a variety of topics, including sample size calculation, stratification, randomization, data systems design, consent forms, publication policies, and ethical standards in clinical trials.
- Q: Is this book suitable for beginners in clinical research? A: While the book provides valuable insights and information, it is best suited for those with a foundational understanding of clinical research, including clinicians, biostatisticians, and epidemiologists.
- Q: What format is the book available in? A: The book is available in hardcover format, providing durability and a professional appearance.
- Q: Does the book include practical examples or resources? A: Yes, the book includes numerous tables, checklists, charts, and other resources that are useful for trialists in the field.
- Q: Can this book assist in understanding current practices in clinical trials? A: Yes, the second edition discusses recent changes and improvements in clinical trial methods, policies, and guidelines, making it relevant for current practices.
- Q: Is this book a good reference for data sharing and ethical standards? A: Absolutely, the book addresses current practices related to data sharing, gender representation, treatment effects monitoring, and ethical standards in clinical trials.