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crossover study

33 papers and 3 presentations; 32 titles.

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Conference × Year × Title × Authors Extras Pages
PHUSE EU 2024 Comparison of the Wilcoxon-Signed Rank Test with the Hodges-Lehmann Estimator in SAS, R and StatXact as Part of the PHUSE CAMIS Project Agnieszka Tomczyk,
Lyn Taylor		 source
presentation source		 7
PharmaSUG 2022 Merging Pharmacokinetic (PK) Sample Collection and Dosing Information for PK Analysis based on Study Design and lessons learned Durga Kalyani Paturi source 11
PHUSE US 2022 Safety ADaM Automation from Design to Implementation [presentation] Chengxin Li,
Toshio Kimura		 source
video		 18
PHUSE US 2021 Industry Metrics for Extensions of CDISC Terminology [presentation] Sergiy Sirichenko source
video		 36
PHUSE EU 2019 Analysis of crossover studies in patient narratives Rebecca Lyzinski source
presentation source		 6
PHUSE EU 2019 Bioequivalence Testing for Highly Variable Drug Products (HVDPs) James R. Johnson source
presentation source		 9
PharmaSUG 2019 Practical Guide for Creating ADaM Datasets in Cross-over Studies Neha Sakhawalkar,
Kamleshkumar Patel		 source 10
PHUSE US 2019 Modeling Safety Pharmacology Study Designs in SEND: An Analysis of a Proof-of-Concept Dataset Kevin Snyder source
presentation source		 5
MWSUG 2018 Avoiding Sinkholes: Common Mistakes During ADaM Data Set Implementation Richann J. Watson 15
PharmaSUG 2018 Avoiding Sinkholes: Common Mistakes During ADaM Data Set Implementation Richann J. Watson,
Karl Miller		 source 18
WUSS 2017 Avoiding Sinkholes: Common Mistakes During ADaM Data Set Implementation Richann J. Watson,
Karl Miller		 source 15
PharmaSUG CN 2017 How to define Treatment Emergent Adverse Event (TEAE) in crossover clinical trials Mengya Yin,
Wen Tan		 6
PharmaSUG 2017 How to define Treatment Emergent Adverse Event (TEAE) in crossover clinical trials Mengya Yin,
Wen Tan		 source 6
SESUG 2016 SDTM What? ADaM Who? A Programmer's Introduction to CDISC Venita DePuy source 9
PHUSE EU 2016 Cross-over to High Quality Graphics: Using SGRENDER to Enhance Graphics in a Cross-Over Study [presentation] Martin Clancy,
Simon Clancy,
Sue McKendrick,
Utpal Sanki		 source
presentation
presentation source		 1
PharmaSUG 2016 Implementation of ADaM Basic Data Structure for Cross-over Studies Songhui Zhu source 10
PharmaSUG 2016 TRTP and TRTA in BDS Application per CDISC ADaM Standards Maggie Ci Jiang source 8
SESUG 2015 Multilevel Randomization Marina Komaroff,
Lois Lynn		 source 10
PharmaSUG 2015 Implementing Various Baselines for ADaM BDS datasets Songhui Zhu source 7
PharmaSUG 2015 Multilevel Randomization Marina Komaroff,
Lois Lynn		 source 10
SESUG 2014 SDTM What? ADaM Who? A Programmer's Introduction to CDISC Venita DePuy source 9
SGF 2011 Repeated Measures Analysis of Correlated Data with Multiple Responses Using SAS Anbuchelvi Jeyabslasingham,
Anpalaki J. Ragavan		 source 10
PharmaSUG 2010 From SAP to ADaM: The Nuts and Bolts Nancy Brucken,
Paul K. Slagle		 9
PharmaSUG 2010 Linear Mixed Models in Clinical Trials using PROC MIXED Danyang Bing,
Xiaomin He		 12
PharmaSUG 2010 Using SAS Proc Power to Perform Model-based Power Analysis for Clinical Pharmacology Studies Peng Sun 11
PHUSE EU 2006 Partial Dates; decisions and implications of handling partially missing dates Rachel Bowman source 6
PharmaSUG 2006 Estimate Carryover Effect in Clinical Trial Crossover Designs David Shen,
Zaizai Lu		 7
PharmaSUG 2005 Assigning Treatment Group in Cross-over Studies: A Practical Approach Charles Ling,
Shulin Yuan		 3
PharmaSUG 2004 SAS Application in 2x2 Crossover Clinical Trial Wuwei Wayne Feng 10
NESUG 1997 Estimation of Direct, Period and Carryover Effects in Crossover Studies Mitchell Kotler 7
SUGI 1997 Graphical and Analytical Tools for the Analysis of Two-Period Crossover Clinical Trials Jeff A. Sloan,
Paul J. Novotny,
Charles L. Loprinzi,
Suresh Nair		 source
MWSUG 1994 Use of Macros in Generating Statistical Comparisons for Bioequivalence Reports A. David Mundt 9
SUGI 1992 An Interactive SAS/AF System for Assessing Bioequivalence Deborah Dukovic source 6
SEUGI 1991 Confidence Intervals for Bioequivalence Studies B. Jones,
D. J. Nichols,
P. Blood		 source 12
SUGI 1991 A SAS Macro for the Robust Analysis of Repeated Measures Data Joe DiGennaro,
William J. Huster		 source 6
SUGI 1990 The Analysis of Data from 2 X 2 Crossover Trials with Baseline Measurements Joe DiGennaro,
William C. Huster		 source 6

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