The Resource Developments in Statistical Evaluation of Clinical Trials, edited by Kees van Montfort, Johan Oud, Wendimagegn Ghidey, (electronic resource)

Developments in Statistical Evaluation of Clinical Trials, edited by Kees van Montfort, Johan Oud, Wendimagegn Ghidey, (electronic resource)

Label
Developments in Statistical Evaluation of Clinical Trials
Title
Developments in Statistical Evaluation of Clinical Trials
Statement of responsibility
edited by Kees van Montfort, Johan Oud, Wendimagegn Ghidey
Creator
Contributor
Editor
Provider
Subject
Language
eng
Summary
This book describes various ways of approaching and interpreting the data produced by clinical trial studies, with a special emphasis on the essential role that biostatistics plays in clinical trials. Over the past few decades the role of statistics in the evaluation and interpretation of clinical data has become of paramount importance. As a result the standards of clinical study design, conduct and interpretation have undergone substantial improvement. The book includes 18 carefully reviewed chapters on recent developments in clinical trials and their statistical evaluation, with each chapter providing one or more examples involving typical data sets, enabling readers to apply the proposed procedures. The chapters employ a uniform style to enhance comparability between the approaches
http://library.link/vocab/creatorName
van Montfort, Kees
Image bit depth
0
LC call number
QA276-280
Literary form
non fiction
http://library.link/vocab/relatedWorkOrContributorName
  • Oud, Johan.
  • Ghidey, Wendimagegn.
  • SpringerLink
http://library.link/vocab/subjectName
  • Statistics
  • Statistical methods
  • Mathematical statistics
  • Statistics
  • Statistical Theory and Methods
  • Statistics for Life Sciences, Medicine, Health Sciences
  • Biostatistics
Label
Developments in Statistical Evaluation of Clinical Trials, edited by Kees van Montfort, Johan Oud, Wendimagegn Ghidey, (electronic resource)
Instantiates
Publication
Antecedent source
mixed
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
not applicable
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
Preface -- List of contributors -- 1.Statistical Models and Methods for Incomplete Data in Randomized Clinical Trials. M.A. McIsaac and R.J. Cook -- 2.Bayesian Decision Theory and the Design and Analysis of Randomized Clinical Trials. A.R. Willan -- 3.Designing Multi-Arm Multi-Stage Clinical Studies. T.Jaki -- 4.Statistical Approaches to Improving Trial Efficiency and Conduct. J.Pogue, P. J. Devereaux and S.Yusuf -- 5.Competing Risk and Survival Analysis. K.van Montfort, P.Fennema and W.Ghidey.- 6.Recent Developments in Group-Sequential Designs. J.M. S. Wason -- 7.Statistical Inference for Non-Inferiority of a Diagnostic Procedure Compared to an Alternative Procedure, Based on the Difference in Correlated Proportions from Multiple Raters. H.Saeki and T.Tango -- 8.Design and Analysis of Clinical Trial Simulations. K.Kuribayashi -- 9.Causal Effect Estimation and Dose Adjustment in Exposure-Response Relationship Analysis. J.Wang -- 10.Different Methods to Analyse Results of a Randomised Controlled Trial with More Than one Follow-up Measurement. J.W. R. Twisk -- 11.Statistical Methods for the Assessment of Clinical Relevance. M.Kieser -- 12.Statistical Considerations in the Use of Composite Endpoints in Time to Event Analyses. R.J. Cook and K.-A.Lee -- 13.Statistical Validation of Surrogate Markers in Clinical Trials. A.Alonso, G.Molenberghs and G.van Breukelen -- 14.Biomarker-Based Designs of Phase III Clinical Trials for Personalized Medicine. S.Matsui, T.Nonaka and Y.Choai -- 15.Dose-Finding Models for Two-Agent Combination Phase I Trials. A.Hirakawa and S.Matsui -- 16.Multi-State Models Used in Oncology Trials. B.Gaschler-Markefski, K.Schiefele, J.Hocke and F.Fleischer -- 17.Review of Designs for Accommodating Patients’ or Physicians’ Preferences in Randomized Controlled Trials. A.S. Ismaila and S.D. Walter -- 18.Dose Finding Methods in Oncology: From the Maximum Tolerated Dose to the Recommended Phase II Dose. X.Paoletti and A.Doussau
Dimensions
unknown
Extent
XI, 361 p. 61 illus.
File format
multiple file formats
Form of item
electronic
Isbn
9783642553455
Level of compression
uncompressed
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other control number
10.1007/978-3-642-55345-5
Other physical details
online resource.
Quality assurance targets
absent
Reformatting quality
access
Specific material designation
remote
System control number
(DE-He213)978-3-642-55345-5
Label
Developments in Statistical Evaluation of Clinical Trials, edited by Kees van Montfort, Johan Oud, Wendimagegn Ghidey, (electronic resource)
Publication
Antecedent source
mixed
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Color
not applicable
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
Preface -- List of contributors -- 1.Statistical Models and Methods for Incomplete Data in Randomized Clinical Trials. M.A. McIsaac and R.J. Cook -- 2.Bayesian Decision Theory and the Design and Analysis of Randomized Clinical Trials. A.R. Willan -- 3.Designing Multi-Arm Multi-Stage Clinical Studies. T.Jaki -- 4.Statistical Approaches to Improving Trial Efficiency and Conduct. J.Pogue, P. J. Devereaux and S.Yusuf -- 5.Competing Risk and Survival Analysis. K.van Montfort, P.Fennema and W.Ghidey.- 6.Recent Developments in Group-Sequential Designs. J.M. S. Wason -- 7.Statistical Inference for Non-Inferiority of a Diagnostic Procedure Compared to an Alternative Procedure, Based on the Difference in Correlated Proportions from Multiple Raters. H.Saeki and T.Tango -- 8.Design and Analysis of Clinical Trial Simulations. K.Kuribayashi -- 9.Causal Effect Estimation and Dose Adjustment in Exposure-Response Relationship Analysis. J.Wang -- 10.Different Methods to Analyse Results of a Randomised Controlled Trial with More Than one Follow-up Measurement. J.W. R. Twisk -- 11.Statistical Methods for the Assessment of Clinical Relevance. M.Kieser -- 12.Statistical Considerations in the Use of Composite Endpoints in Time to Event Analyses. R.J. Cook and K.-A.Lee -- 13.Statistical Validation of Surrogate Markers in Clinical Trials. A.Alonso, G.Molenberghs and G.van Breukelen -- 14.Biomarker-Based Designs of Phase III Clinical Trials for Personalized Medicine. S.Matsui, T.Nonaka and Y.Choai -- 15.Dose-Finding Models for Two-Agent Combination Phase I Trials. A.Hirakawa and S.Matsui -- 16.Multi-State Models Used in Oncology Trials. B.Gaschler-Markefski, K.Schiefele, J.Hocke and F.Fleischer -- 17.Review of Designs for Accommodating Patients’ or Physicians’ Preferences in Randomized Controlled Trials. A.S. Ismaila and S.D. Walter -- 18.Dose Finding Methods in Oncology: From the Maximum Tolerated Dose to the Recommended Phase II Dose. X.Paoletti and A.Doussau
Dimensions
unknown
Extent
XI, 361 p. 61 illus.
File format
multiple file formats
Form of item
electronic
Isbn
9783642553455
Level of compression
uncompressed
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other control number
10.1007/978-3-642-55345-5
Other physical details
online resource.
Quality assurance targets
absent
Reformatting quality
access
Specific material designation
remote
System control number
(DE-He213)978-3-642-55345-5

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