Factors influencing the statistical planning, design, conduct, analysis and reporting of trials in health care: A systematic review
暂无分享,去创建一个
[1] D. Devane,et al. A protocol for a systematic review investigating the factors influencing the statistical planning, design, conduct, analysis and reporting of trials , 2020, HRB open research.
[2] K. Walters,et al. New Horizons in the use of routine data for ageing research , 2020, Age and ageing.
[3] Diane D. Liu,et al. Bayesian clinical trials at The University of Texas MD Anderson Cancer Center: An update , 2019, Clinical trials.
[4] T. Eliades,et al. Methods, transparency and reporting of clinical trials in orthodontics and periodontics , 2019, Journal of orthodontics.
[5] A. Goldkorn,et al. Development of a translational medicine protocol for an NCTN genitourinary clinical trial: Critical steps, common pitfalls and a basic guide to translational clinical research. , 2019, Urologic oncology.
[6] H. Barnhart,et al. Working With Statisticians in Clinical Research , 2018, Stroke.
[7] Lisa V. Hampson,et al. Adaptive designs in clinical trials: why use them, and how to run and report them , 2018, BMC Medicine.
[8] S. Lewis,et al. Guidelines for the Content of Statistical Analysis Plans in Clinical Trials , 2017, JAMA.
[9] Sean M. O'Brien,et al. How well does early‐career investigators’ cardiovascular outcomes research training align with funded outcomes research? , 2017, American heart journal.
[10] Rory Wilson,et al. Towards evidence-based computational statistics: lessons from clinical research on the role and design of real-data benchmark studies , 2017, BMC Medical Research Methodology.
[11] D. DeMets,et al. Recommendations for data monitoring committees from the Clinical Trials Transformation Initiative , 2017, Clinical trials.
[12] D. DeMets,et al. Data monitoring committees: Promoting best practices to address emerging challenges , 2017, Clinical trials.
[13] D. DeMets,et al. Understanding the functions and operations of data monitoring committees: Survey and focus group findings , 2017, Clinical trials.
[14] D. Berry,et al. A conceptual model for the development process of confirmatory adaptive clinical trials within an emergency research network , 2017, Clinical trials.
[15] Hossam M. Hammady,et al. Rayyan—a web and mobile app for systematic reviews , 2016, Systematic Reviews.
[16] D. Berry,et al. Attitudes and opinions regarding confirmatory adaptive clinical trials: a mixed methods analysis from the Adaptive Designs Accelerating Promising Trials into Treatments (ADAPT-IT) project , 2016, Trials.
[17] A. Scrimgeour,et al. Data sharing and the evolving role of statisticians , 2016, BMC Medical Research Methodology.
[18] R. Califf. Pragmatic clinical trials: Emerging challenges and new roles for statisticians , 2016, Clinical trials.
[19] Jonathan H Seltzer,et al. Responsibilities of Data Monitoring Committees: Consensus Recommendations , 2016, Therapeutic innovation & regulatory science.
[20] J. Tyson,et al. Stopping guidelines for an effectiveness trial: what should the protocol specify? , 2016, Trials.
[21] T. Perneger,et al. Patient enrollment and logistical problems top the list of difficulties in clinical research: a cross-sectional survey , 2016, BMC Medical Research Methodology.
[22] P. Sandercock,et al. Exploring the role and function of trial steering committees: results of an expert panel meeting , 2015, Trials.
[23] S. Todd,et al. Cross-sector surveys assessing perceptions of key stakeholders towards barriers, concerns and facilitators to the appropriate use of adaptive designs in confirmatory trials , 2015, Trials.
[24] John Eng,et al. Use of Spreadsheets for Research Data Collection and Preparation: A Primer. , 2015, Academic radiology.
[25] S. Todd,et al. Missing steps in a staircase: a qualitative study of the perspectives of key stakeholders on the use of adaptive designs in confirmatory trials , 2015, Trials.
[26] D. Berry,et al. Reflections on the adaptive designs accelerating promising trials into treatments (ADAPT-IT) process—Findings from a qualitative study , 2015, Clinical research and regulatory affairs.
[27] Alexa McArthur,et al. Innovations in the systematic review of text and opinion , 2015, International journal of evidence-based healthcare.
[28] Hanan Khalil,et al. Summarizing systematic reviews: methodological development, conduct and reporting of an umbrella review approach , 2015, International journal of evidence-based healthcare.
[29] N. Pandis,et al. Reporting quality of randomised controlled trials published in prosthodontic and implantology journals. , 2015, Journal of oral rehabilitation.
[30] K. K. Snow,et al. Processes to manage analyses and publications in a phase III multicenter randomized clinical trial , 2014, Trials.
[31] Jim Euchner. Design , 2014, Catalysis from A to Z.
[32] C. Watkins,et al. Utility values in health technology assessments: a statistician's perspective , 2014, Pharmaceutical statistics.
[33] Julia Y. Lin,et al. Establishing a data monitoring committee for clinical trials , 2014, Shanghai archives of psychiatry.
[34] H. Pang,et al. Methodological considerations in the design and implementation of clinical trials. , 2014, Seminars in oncology nursing.
[35] R. Tibshirani,et al. Increasing value and reducing waste in research design, conduct, and analysis , 2014, The Lancet.
[36] P. Archdeacon,et al. Optimizing Expedited Safety Reporting for Drugs and Biologics Subject to an Investigational New Drug Application , 2013, Therapeutic innovation & regulatory science.
[37] David Morgan,et al. Multiplicity: discussion points from the Statisticians in the Pharmaceutical Industry multiplicity expert group , 2013, Pharmaceutical statistics.
[38] B. Levin,et al. Overview, hurdles, and future work in adaptive designs: perspectives from a National Institutes of Health-funded workshop , 2012, Clinical trials.
[39] Sandy Oliver,et al. Narrative approaches to systematic review and synthesis of evidence for international development policy and practice , 2012 .
[40] N. Pandis,et al. What's in a title? An assessment of whether randomized controlled trial in a title means that it is one. , 2012, American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics.
[41] S. Ellenberg. Protecting Clinical Trial Participants and Protecting Data Integrity: Are We Meeting the Challenges? , 2012, PLoS medicine.
[42] D. Dixon,et al. Data and safety monitoring policy for National Institute of Allergy and Infectious Diseases clinical trials , 2011, Clinical trials.
[43] T. Murphy,et al. Gerontologic Biostatistics: The Statistical Challenges of Clinical Research with Older Study Participants , 2010, Journal of the American Geriatrics Society.
[44] Chul Ahn,et al. Bridging Clinical Investigators and Statisticians , 2009, Journal of Investigative Medicine.
[45] Stephen Senn,et al. Measurement in clinical trials: A neglected issue for statisticians? , 2009, Statistics in medicine.
[46] K. Carroll,et al. Back to basics: explaining sample size in outcome trials, are statisticians doing a thorough job? , 2009, Pharmaceutical statistics.
[47] T. Fleming,et al. Design, Conduct, and Analysis of Clinical Trials in Disease due to Methicillin‐Resistant Staphylococcus aureus , 2009, Clinical pharmacology and therapeutics.
[48] C. Gross,et al. Evaluating the Surgery Literature: Can Standardizing Peer-Review Today Predict Manuscript Impact Tomorrow? , 2009, Annals of surgery.
[49] D. Moher,et al. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement , 2009, BMJ : British Medical Journal.
[50] A. Nierenberg,et al. Integrating Statistical and Clinical Research Elements in Intervention-Related Grant Applications: Summary From an NIMH Workshop , 2009, Academic psychiatry : the journal of the American Association of Directors of Psychiatric Residency Training and the Association for Academic Psychiatry.
[51] Sergio Sismondo,et al. Ghosts in the Machine , 2009, Social studies of science.
[52] A. Harden,et al. Methods for the thematic synthesis of qualitative research in systematic reviews , 2008, BMC medical research methodology.
[53] Trevor Lewis. Professional development of statisticians in the pharmaceutical sector: evolution over the past decade and into the future , 2008, Pharmaceutical statistics.
[54] A. Erdemir,et al. Ethics in a scientific approach: the importance of the biostatistician in research ethics committees , 2008, Journal of Medical Ethics.
[55] R. Hattemer‐Apostel,et al. Getting Better Clinical Trial Data: An Inverted Viewpoint , 2008 .
[56] S. Hughes. European regulatory agencies should employ full time statisticians , 2008, BMJ : British Medical Journal.
[57] Saul Miller,et al. Research Ethics Committee. , 2007 .
[58] U. Harnischmacher,et al. Consequences of Directive 2001/20/EC for investigator-initiated trials in the paediatric population—a field report , 2007, European Journal of Pediatrics.
[59] Marvin Zelen,et al. Biostatisticians, biostatistical science and the future , 2006, Statistics in medicine.
[60] F. Kianifard,et al. Teaching statistics to clinical research staff in a pharmaceutical company , 2006, Pharmaceutical statistics.
[61] V. Braun,et al. Using thematic analysis in psychology , 2006 .
[62] G. Preminger,et al. Clinical research and statistical methods in the urology literature. , 2005, The Journal of urology.
[63] J. Pignon,et al. Clinical research infrastructures and networks in France: report on the French ECRIN workshop. , 2005, The´rapie (Paris).
[64] T. Perneger,et al. Medical researchers evaluate their methodological skills. , 2004, Journal of clinical epidemiology.
[65] R. Califf,et al. Task force 2: Investigator participation in clinical research. , 2004, Journal of the American College of Cardiology.
[66] J. Wittes. Playing safe and preserving integrity: making the FDA model work , 2004, Statistics in medicine.
[67] S. Snapinn,et al. The role of the unblinded sponsor statistician , 2004, Statistics in medicine.
[68] D. DeMets,et al. The independent statistician for data monitoring committees , 2004, Statistics in medicine.
[69] S. George,et al. Should statisticians reporting to data monitoring committees be independent of the trial sponsor and leadership? , 2004, Statistics in medicine.
[70] J. Bryant. What is the appropriate role of the trial statistician in preparing and presenting interim findings to an independent Data Monitoring Committee in the U.S. Cancer Cooperative Group setting? , 2004, Statistics in medicine.
[71] Stuart J Pocock,et al. A major trial needs three statisticians: why, how and who? , 2004, Statistics in medicine.
[72] G. Campbell,et al. Independence of the statistician who analyses unblinded data , 2004, Statistics in medicine.
[73] D. DeMets,et al. Issues in regulatory guidelines for data monitoring committees , 2004, Clinical trials.
[74] Peter F Thall,et al. Ethical issues in oncology biostatistics , 2002, Statistical methods in medical research.
[75] S. Goodman,et al. How statistical expertise is used in medical research. , 2002, JAMA.
[76] A. Grieve. Do statisticians count? A personal view , 2002 .
[77] J Llorca,et al. Participation of epidemiologists and/or biostatisticians and methodological quality of published controlled clinical trials , 2001, Journal of epidemiology and community health.
[78] 서정헌,et al. 반도체 공정 overview , 2001 .
[79] Anneke Grobler,et al. The Role of the Statistician in the Data Management Process , 2001 .
[80] David M. L. Morgan. Qualified Statisticians in the European Pharmaceutical Industry: Report of a European Federation of Statisticians in the Pharmaceutical Industry (EFSPI) Working Group , 1999 .
[81] A. Vail. Experiences of a biostatistician on a U.K. Research Ethics Committee. , 1998, Statistics in medicine.
[82] K. Tsang. Evidence-based medical practice: as viewed by a clinical researcher. , 1998, Hong Kong medical journal = Xianggang yi xue za zhi.
[83] Tosiya Sato,et al. Expectations for an International Harmonized Guideline , 1998 .
[84] A. Munro. Publishing the findings of clinical research. , 1993, British medical journal.
[85] Thomas E. Bradstreet,et al. A Statistics Appreciation Course for Clinical Research Personnel , 1992 .
[86] Ellenberg Jh. Biostatistical collaboration in medical research. , 1990 .
[87] K. James. A model for the development, conduct, and monitoring of multicenter clinical trials in the Veterans Administration. , 1980, Controlled clinical trials.
[88] N. Breslow,et al. Perspectives on the statistician's role in cooperative clinical research , 1978, Cancer.
[89] MARGARET GOWING,et al. A Model of Development , 1973, Nature.
[90] Rspm μgm. Methods , 1972 .
[91] C. Tufanaru,et al. Chapter 7: Systematic Reviews of Etiology and Risk , 2020, JBI Manual for Evidence Synthesis.
[92] S. Todd,et al. Proposed best practice for statisticians in the reporting and publication of pharmaceutical industry‐sponsored clinical trials , 2011, Pharmaceutical statistics.
[93] Susan Todd,et al. The potential for bias in reporting of industry‐sponsored clinical trials , 2011, Pharmaceutical statistics.
[94] Kerry Gordon. Who wants to be an ICH Euro billionaire? , 2008, Pharmaceutical statistics.
[95] J. Popay,et al. Guidance on the conduct of narrative synthesis in sytematic reviews , 2006 .
[96] F. Rockhold. Requiring ‘independent’ statistical analyses for industry sponsored trials? , 2006, Pharmaceutical statistics.
[97] W Maurer,et al. Creative and Innovative Statistics in Clinical Research and Development , 2005, Methods of Information in Medicine.
[98] J. Hutton,et al. Statistical review by research ethics committees , 2000 .
[99] R. Prescott,et al. Factors that limit the quality, number and progress of randomised controlled trials. , 1999, Health technology assessment.