Author: Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 608
Book Description
Compilation of Experimental Cancer Therapy Protocol Summaries
Author: Compilation of Experimental Cancer Therapy Protocol Summaries
Author: Compilation of Cancer Therapy Protocol Summaries
Author: International Cancer Research Data BankPublisher:
ISBN:
Category : Cancer
Languages : en
Pages : 764
Book Description
Compilation of Cancer Therapy Protocol Summaries
Author: Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 738
Book Description
Detailed outlines of ongoing experimental clinical trials. Data may also be retrieved in CLINPROT. Classified arrangement according to site. Each entry gives such information as investigator and address, objective, protocol outline, and dosage schedule. Tumor, agent, and protocol organizational number indexes. Miscellaneous appendixes.
Compilation of Clinical Protocol Summaries
Author: Smithsonian Science Information Exchange. Current Cancer Research Project Analysis CenterPublisher:
ISBN:
Category : Cancer
Languages : en
Pages : 412
Book Description
Compilation of Clinical Protocol Summaries
Author: International Cancer Research Data BankPublisher:
ISBN:
Category : Cancer
Languages : en
Pages : 395
Book Description
The Prevention and Treatment of Missing Data in Clinical Trials
Author: National Research CouncilPublisher: National Academies Press
ISBN: 030918651X
Category : Medical
Languages : en
Pages : 163
Book Description
Randomized clinical trials are the primary tool for evaluating new medical interventions. Randomization provides for a fair comparison between treatment and control groups, balancing out, on average, distributions of known and unknown factors among the participants. Unfortunately, these studies often lack a substantial percentage of data. This missing data reduces the benefit provided by the randomization and introduces potential biases in the comparison of the treatment groups. Missing data can arise for a variety of reasons, including the inability or unwillingness of participants to meet appointments for evaluation. And in some studies, some or all of data collection ceases when participants discontinue study treatment. Existing guidelines for the design and conduct of clinical trials, and the analysis of the resulting data, provide only limited advice on how to handle missing data. Thus, approaches to the analysis of data with an appreciable amount of missing values tend to be ad hoc and variable. The Prevention and Treatment of Missing Data in Clinical Trials concludes that a more principled approach to design and analysis in the presence of missing data is both needed and possible. Such an approach needs to focus on two critical elements: (1) careful design and conduct to limit the amount and impact of missing data and (2) analysis that makes full use of information on all randomized participants and is based on careful attention to the assumptions about the nature of the missing data underlying estimates of treatment effects. In addition to the highest priority recommendations, the book offers more detailed recommendations on the conduct of clinical trials and techniques for analysis of trial data.
Protocol Handbook for Cancer Biology
Author: Gauri MisraPublisher: Academic Press
ISBN: 0323898173
Category : Science
Languages : en
Pages : 222
Book Description
Protocol Handbook for Cancer Biology brings together a comprehensive collection of the methods used for cancer assessment, diagnostics, and therapeutics. Various protocols are discussed along with alternative strategies, including the advantages and limitations of techniques that have been used in labs globally. These protocols are presented by cancer biology experts based on their real-world experience. The protocols in this book will be a valuable resource for cancer researchers and graduate students, who can utilize the techniques described to conduct research more efficiently and successfully. Presents comprehensive protocols used for cancer assessment, diagnostics, and therapeutics all in one place Encompasses alternative strategies considering the requirements of the end user and taking into consideration diverse research settings Discusses limitations and advantages of each method in experimental design and execution, thus saving time during the research process
Transforming Clinical Research in the United States
Author: Institute of MedicinePublisher: National Academies Press
ISBN: 0309163358
Category : Medical
Languages : en
Pages : 151
Book Description
An ideal health care system relies on efficiently generating timely, accurate evidence to deliver on its promise of diminishing the divide between clinical practice and research. There are growing indications, however, that the current health care system and the clinical research that guides medical decisions in the United States falls far short of this vision. The process of generating medical evidence through clinical trials in the United States is expensive and lengthy, includes a number of regulatory hurdles, and is based on a limited infrastructure. The link between clinical research and medical progress is also frequently misunderstood or unsupported by both patients and providers. The focus of clinical research changes as diseases emerge and new treatments create cures for old conditions. As diseases evolve, the ultimate goal remains to speed new and improved medical treatments to patients throughout the world. To keep pace with rapidly changing health care demands, clinical research resources need to be organized and on hand to address the numerous health care questions that continually emerge. Improving the overall capacity of the clinical research enterprise will depend on ensuring that there is an adequate infrastructure in place to support the investigators who conduct research, the patients with real diseases who volunteer to participate in experimental research, and the institutions that organize and carry out the trials. To address these issues and better understand the current state of clinical research in the United States, the Institute of Medicine's (IOM) Forum on Drug Discovery, Development, and Translation held a 2-day workshop entitled Transforming Clinical Research in the United States. The workshop, summarized in this volume, laid the foundation for a broader initiative of the Forum addressing different aspects of clinical research. Future Forum plans include further examining regulatory, administrative, and structural barriers to the effective conduct of clinical research; developing a vision for a stable, continuously funded clinical research infrastructure in the United States; and considering strategies and collaborative activities to facilitate more robust public engagement in the clinical research enterprise.
Directory of Cancer Research Information Resources
Author: Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 284
Book Description
Available cancer information sources throughout the world. Includes publications, libraries, classification schemes, audiovisual sources, cancer registries, special collections, projects information sources, organizations, and government agencies. Classified arrangement. Each entry gives descriptive and contact information. Title, organization, geographical, and subject indexes. Bibliography of 99 references.
