Fundamentals of clinical trials / Lawrence M.Friedman, Curt D. Furberg, David L. DeMets

Por: Friedman, LawrenceTipo de material: TextoTextoDetalles de publicación: New York : Springer, 1998 Edición: 3rd ed.Descripción: 361 p. : il. ; 24 cmISBN: 0-387-98586-7Tema(s): Clinical trials | Research design | Ensayos clínicos | Diseño experimentalResumen: INDICE: Introduction to clinical trials. What is the question?. Study population. Basic study design. The randomization process. Blindness. Sample size. Baseline assessment. Recruiment of study participants. Data collection and quality control. Assessing and reporting adverse effects. Assessment of health-related quality of life. Participant adherence. Survival analysis. Monitoring response variables. Issues in data analysis. Closeout. Reporting and interpreting of results... Etc.Resumen: Índice: Introduction to clinical trials. What is the question?. Study population. Basic study design. The randomization process. Blindness. Sample size. Baseline assessment. Recruiment of study participants. Data collection and quality control. Assessing and reporting adverse effects. Assessment of health-related quality of life. Participant adherence. Survival analysis. Monitoring response variables. Issues in data analysis. Closeout. Reporting and interpreting of results. Multicenter trials. Index
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INDICE: Introduction to clinical trials. What is the question?. Study population. Basic study design. The randomization process. Blindness. Sample size. Baseline assessment. Recruiment of study participants. Data collection and quality control. Assessing and reporting adverse effects. Assessment of health-related quality of life. Participant adherence. Survival analysis. Monitoring response variables. Issues in data analysis. Closeout. Reporting and interpreting of results... Etc.

Índice: Introduction to clinical trials. What is the question?. Study population. Basic study design. The randomization process. Blindness. Sample size. Baseline assessment. Recruiment of study participants. Data collection and quality control. Assessing and reporting adverse effects. Assessment of health-related quality of life. Participant adherence. Survival analysis. Monitoring response variables. Issues in data analysis. Closeout. Reporting and interpreting of results. Multicenter trials. Index

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