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ISSN: 2333-9721
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Clinical Trials

ISSN Print: 1740-7745

ISSN Online: 1740-7753

主页: https://journals.sagepub.com/loi/ctja

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Displaying 1- 50 out of 118 articles       1  |  2  |  3  |    Page. /3 Go

Comprehension and recall from the informed consent process by phase I healthy volunteers before dose administration

Gillian E Caughey,Rami Tadros,Sally Johns,Sepehr Shakib

Making the case for completion bonuses in clinical trials

Emily A Largent,Holly Fernandez Lynch

Commentary on Hay et al.: Can clinical trials data collection be improved by administrative data elements?

Kip Brown,Micha？l Chassé

Merged block randomisation: A novel randomisation procedure for small clinical trials

Stéphanie L van der Pas

Determination of fasiglifam

Abhinav Sharma,Christopher B Granger,David Holmes,James Neaton,Jay S Shavadia,Laurie DeLeve,Paul B Watkins,Phillip Home,Robert H Eckel,Xiangqiong Gu

Transitioning to the National Institutes of Health single institutional review board model: Piloting the use of the Streamlined, Multi

Adrian F Hernandez,Amy Franklin,Barbara E Bierer,Lauren W. Cohen,Mina Baqai,Nichelle Cobb,Orly Vardeny,Sarah Palmer

Exploring the roots of clinical trial methodology in medieval Islamic medicine

Mahdi Zarvandi,Ramin Sadeghi

Editorial: We may need large trials to find treatments for neurodegenerative diseases

David Alan Schoenfeld,Michael Benatar

The development of an end

Abbey Child,Jodie Allen,Sarah Mertens

There is still a place for significance testing in clinical trials

Colin B Begg,Dean A Fergusson,Edward L Korn,Ian Ford,Jonathan A Cook,Jonathan Kimmelman,Mithat Gonen

Investigational drug labeling variability

Amélie Duhamel,Cynthia Tanguay,Denis Lebel,Jean-Fran？ois Bussières,Maxime Thibault

Commentary on Diamond et al.: The efficiency of single institutional review board review in National Institute of Child Health and Human Development Cooperative Reproductive Medicine Network–initiated clinical trials

Robert Klitzman

2018 Peer Reviewers, 2019

null

Shift models for dose

Bethany Jablonski Horton,Mark R Conaway,Nolan A Wages

Corrigendum, 2019

null

Conditional estimation and inference to address observed covariate imbalance in randomized clinical trials

Chunling Liu,Linli Tang,Vance W Berger,Zhiwei Zhang

Challenges and solutions in the design and execution of the PROSPECT Phase II/III neoadjuvant rectal cancer trial (NCCTG N1048/Alliance)

Alan Venook,Deborah Schrag,Ethan Basch,Harvey Mamon,Leonard Saltz,Marc Gollub,Martin Weiser,Qian Shi

Beware of on

Bertram Pitt,Fred Yang,Janet Wittes

Generalizing the per

Daniel Westreich,Enrique F Schisterman,H Irene Hall,Haidong Lu,Jessie K Edwards,Stephen R Cole,Tiffany L Breger

Conducting clinical trials—costs, impacts, and the value of clinical trials networks: A scoping review

Colene Bentley,Janet Dancey,Karen Arts,Kim van der Hoek,Sonya Cressman,Stuart Peacock

Sample size calculation for stepped

Anita Huis,Anja Haenen,Femke Atsma,Laura Rodwell,Marlies Hulscher,Monica Taljaard,Steven Teerenstra

Pilot study of the ability to probabilistically link clinical trial patients to administrative data and determine long

Annette E Hay,Chris O’Callaghan,Craig C Earle,Dongsheng Tu,Elyse Corn,Erin N Bell,Joseph L Pater,Lei Han,Nelson Chong,Ximena Camacho

Caregiver

Francis J Keefe,Gregory Samsa,Janet Bull,Jennifer L Steel,Laura C Hanson,Laura S Porter,Stacy Fischer,Thomas W LeBlanc

Establishing an electronic health record–supported approach for outreach to and recruitment of persons at high risk of type 2 diabetes in clinical trials: The vitamin D and type 2 diabetes (D2d) study experience

Anastassios G Pittas,Chhavi Chadha,Cyrus Desouza,Ellen M Vickery,Erin S LeBlanc,Irwin G Brodsky,Lawrence S Phillips,Miranda G Ouellette,Myrlene A Staten,Patricia R Sheehan,Ranee Chatterjee,Vanita R Aroda,null

A readily available improvement over method of moments for intra

Philip M Westgate

Automated safety event monitoring using electronic medical records in a clinical trial setting: Validation study using the VA NEPHRON

Gary R Johnson,Jane H Zhang,Linda F Fried,Linda Mcdonald,Susannah Chiu,Tassos C Kyriakides,Yuan Huang

Assessing the impact of efficacy stopping rules on the error rates under the multi

Alexandra Blenkinsop,Babak Choodari-Oskooei,Mahesh KB Parmar

Commentary on King

Allison Barz Leahy,Ethan Basch

Comment on Vickers et al.

Rick Chappell

Patient reported outcomes in anti

Bellinda L King-Kallimanis,Gideon M Blumenthal,Harpreet Singh,Jessica K Roydhouse,Lynn J Howie,Marc R Theoret,Paul G Kluetz

The design and conduct of Project RedDE: A cluster

Christoph U Lehmann,David G Bundy,Elizabeth Rice-Conboy,Hardeep Singh,Heather C O’Donnell,Michael L Rinke,Moonseong Heo,Ruth EK Stein,Tammy M Brady

Variance prior specification for a basket trial design using Bayesian hierarchical modeling

Alexia Iasonos,Kristen M Cunanan,Mithat G？nen,Ronglai Shen

Developing a risk

Daniel F Hanley,Donald J Brambilla,Harold P Lehmann,James F Casella,James Tonascia,Jenifer H Voeks,John J Strouse,Krista Vermillion,Pia Maier,Rachel Dlugash,Radhika Avadhani,Richard E Thompson,Robert J Adams

The efficiency of single institutional review board review in National Institute of Child Health and Human Development Cooperative Reproductive Medicine Network–initiated clinical trials

Anne Z Steiner,Christos Coutifaris,Esther Eisenberg,Hao Huang,Heping Zhang,JC Trussell,Karl R Hansen,Kate Maurer,Kurt Barnhart,Marcelle Cedars,Michael P Diamond,Nanette Santoro,Richard S Legro,Robert A Wild,Stephen A Krawetz,Tracey R Thomas,Tracy Ziolek,null

Strategic inclusion of regions in multiregional clinical trials

Deborah Chee,EunYoung Kim,Seung Yeon Song

FDA

Cheryl McMahill-Walraven,Christopher B Granger,Crystal Garcia,David Martin,Debbe McCall,Hussein R Al-Khalidi,Jennifer C Goldsack,Kevin Haynes,Lauren Parlett,Nancy D Lin,Noelle M Cocoros,Patrick Archdeacon,Richard Platt,Robert Temple,Sana M Al-Khatib,Sean D Pokorney,Thomas Harkins,Vinit Nair

Routinely collected data for trialists: The need for continued conversations and solution sharing

Fiona V Lugg-Widger,Michael Robling

Response to Chappell

Andrew J Vickers,Behfar Ehadaie

Inference on covariate effect types for treatment effectiveness in a randomized trial with a binary outcome

Yasutaka Chiba

Improving pragmatic clinical trial design using real

Andrea J Cook,Carolyn M Rutter,Gregory E Simon,Susan M Shortreed

Use of telephone and web interfaces of interactive response technology at clinical investigator sites in clinical trials

Anja Walzer,Anna-Leena Saarela,Anne Mari Juppo

Design and sample size considerations for Alzheimer’s disease prevention trials using multistate models

Nada Abdalla,Ron Brookmeyer

Globalization of clinical trials: Variation in estimated regional costs of pivotal trials, 2015–2016

G Caleb Alexander,Thomas J Moore,Yao Qiao

A review of the impact of utilising electronic medical records for clinical research recruitment

Janyne Dawn Afseth,Yan See Lai

Cost

Mirjam Moerbeek

Barriers and facilitators to clinical trial participation among parents of children with pediatric neuromuscular disorders

Aad Tibben,Barbara B Biesecker,Benjamin S Wilfond,Diana M Escolar,Holly L Peay,Jill Jarecki,Kendall L Umstead

Expedited and facilitated drug evaluations and evidence of benefit and risk: The cup is half

Robert M Califf

TwiC or treat? Are trials within cohorts ethically defensible?

Charles Weijer,Cory E Goldstein,Monica Taljaard

Time to institutional review board approval with local versus central review in a multicenter pragmatic trial

Lakisha J Gaskins,Mark D Neuman,Tracy Ziolek,null

A systematic review and development of a classification framework for factors associated with missing patient

Harriet Richardson,Madeleine King,Melanie Calvert,Michael Brundage,Michael J Palmer,Rebecca Mercieca-Bebber

Displaying 1- 50 out of 118 articles       1  |  2  |  3  |    Page. /3 Go




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