evaluating clinical research
Bengt D. Furberg () and
Curt D. Furberg ()
Additional contact information
Bengt D. Furberg: Associate Professor
Curt D. Furberg: Wake Forest University School of MedicineMedical Center Boulevard, Division of Public Health Sciences
in Springer Books from Springer
Date: 2007
ISBN: 978-0-387-72899-5
References: Add references at CitEc
Citations:
There are no downloads for this item, see the EconPapers FAQ for hints about obtaining it.
Chapters in this book:
- Ch Chapter 1 What is the purpose of this book?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 10 Why is blinding/masking so important?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 11 How is symptomatic improvement measured?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 12 Is it really possible to assess quality of life?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 13 What is the value of biologic markers in drug evaluation?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 14 How are adverse drug reactions measured?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 15 How representative are study subjects in clinical trials?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 16 What happened to the study subjects who disappeared from the analysis?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 17 How reliable are active-control trials?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 18 How informative are composite outcomes?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 19 Do changes in biologic markers predict clinical benefit?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 2 Why is benefit-to-harm balance essential to treatment decisions?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 20 How trustworthy are the authors?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 21 Does publication in a reputable scientific journal guarantee quality?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 22 Is it necessary to be a biostatistician to interpret scientific data?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 23 Are all drugs of a class interchangeable?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 24 How much confidence can be placed on economic analysis?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 25 How should I handle the massive flow of information?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 26 How well is research translated into clinical care?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 3 What are the strengths of randomized controlled clinical trials?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 4 What are the weaknesses of randomized controlled clinical trials?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 5 Do meta-analyses provide the ultimate truth?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 6 What are the strengths of observational studies?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 7 What are the weaknesses of observational studies?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 8 Were the scientific questions stated in advance?
- Bengt D. Furberg and Curt D. Furberg
- Ch Chapter 9 Were the treatment groups comparable initially?
- Bengt D. Furberg and Curt D. Furberg
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:spr:sprbok:978-0-387-72899-5
Ordering information: This item can be ordered from
http://www.springer.com/9780387728995
DOI: 10.1007/978-0-387-72899-5
Access Statistics for this book
More books in Springer Books from Springer
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().