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Integrating Clinical Research into Epidemic Response - The Ebola Experience (Paperback) Loot Price: R2,045
Discovery Miles 20 450
Integrating Clinical Research into Epidemic Response - The Ebola Experience (Paperback): National Academies of Sciences,...

Integrating Clinical Research into Epidemic Response - The Ebola Experience (Paperback)

National Academies of Sciences, Engineering, and Medicine, Health and Medicine Division, Board on Health Sciences Policy, Board on Global Health, Committee on Clinical Trials During the 2014-2015 Ebola Outbreak; Edited by Emily R. Busta, Michelle Mancher, Patricia A. Cuff, Keith McAdam, Gerald Keusch

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Loot Price R2,045 Discovery Miles 20 450 | Repayment Terms: R192 pm x 12*

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The 2014?2015 Ebola epidemic in western Africa was the longest and most deadly Ebola epidemic in history, resulting in 28,616 cases and 11,310 deaths in Guinea, Liberia, and Sierra Leone. The Ebola virus has been known since 1976, when two separate outbreaks were identified in the Democratic Republic of Congo (then Zaire) and South Sudan (then Sudan). However, because all Ebola outbreaks prior to that in West Africa in 2014?2015 were relatively isolated and of short duration, little was known about how to best manage patients to improve survival, and there were no approved therapeutics or vaccines. When the World Heath Organization declared the 2014-2015 epidemic a public health emergency of international concern in August 2014, several teams began conducting formal clinical trials in the Ebola affected countries during the outbreak. Integrating Clinical Research into Epidemic Response: The Ebola Experience assesses the value of the clinical trials held during the 2014?2015 epidemic and makes recommendations about how the conduct of trials could be improved in the context of a future international emerging or re-emerging infectious disease events. Table of Contents Front Matter Summary 1 Introduction 2 Conducting Clinical Research During an Epidemic 3 Assessment of Therapeutic Trials 4 Assessment of Vaccine Trials 5 Strengthening Capacity for Response and Research 6 Engaging Communities in Research and Response 7 Facilitating International Coordination and Collaboration Appendix A: Study Approach and Methods Appendix B: Clinical Trial Designs Appendix C: Ethical Principles for Research with Human Subjects Appendix D: Biographical Sketches of Committee Members and Staff

General

Imprint: National Academies Press
Country of origin: United States
Release date: July 2017
First published: 2017
Authors: National Academies of Sciences, Engineering, and Medicine • Health and Medicine Division • Board on Health Sciences Policy • Board on Global Health • Committee on Clinical Trials During the 2014-2015 Ebola Outbreak
Editors: Emily R. Busta • Michelle Mancher • Patricia A. Cuff • Keith McAdam • Gerald Keusch
Dimensions: 229 x 152mm (L x W)
Format: Paperback
Pages: 342
ISBN-13: 978-0-309-45776-7
Categories: Books > Medicine > General issues > Public health & preventive medicine > General
Books > Medicine > Other branches of medicine > Accident & emergency medicine > General
Books > Medicine > Clinical & internal medicine > Diseases & disorders > Infectious & contagious diseases > General
LSN: 0-309-45776-9
Barcode: 9780309457767

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