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Artykuły w czasopismach na temat "Trials"
Seow, Hsien-Yeang, Patrick Whelan, Mark N. Levine, Kathryn Cowan, Barbara Lysakowski, Brenda Kowaleski, Anne Snider, Rebecca Y. Xu i Andrew Arnold. "Funding Oncology Clinical Trials: Are Cooperative Group Trials Sustainable?" Journal of Clinical Oncology 30, nr 13 (1.05.2012): 1456–61. http://dx.doi.org/10.1200/jco.2011.37.2698.
Pełny tekst źródłaVan Der Weyden, Martin B. "Trials on trial". Medical Journal of Australia 175, nr 5 (wrzesień 2001): 241. http://dx.doi.org/10.5694/j.1326-5377.2001.tb143553.x.
Pełny tekst źródłaNelson, Mark. "Trials on trial". New Scientist 209, nr 2800 (luty 2011): 30. http://dx.doi.org/10.1016/s0262-4079(11)60384-9.
Pełny tekst źródłaVulto, Arnold G. "Clinical trials on trial". European Journal of Hospital Pharmacy 19, nr 4 (sierpień 2012): 347. http://dx.doi.org/10.1136/ejhpharm-2012-000180.
Pełny tekst źródłaPimentel, Leonardo Duarte, Claudio Horst Bruckner, Candida Elisa Manfio, Sérgio Yoshimitsu Motoike i Hermínia Emília Prieto Martinez. "SUBSTRATE, LIME, PHOSPHORUS AND TOPDRESS FERTILIZATION IN MACAW PALM SEEDLING PRODUCTION". Revista Árvore 40, nr 2 (kwiecień 2016): 235–44. http://dx.doi.org/10.1590/0100-67622016000200006.
Pełny tekst źródłade Vries, Ymkje Anna, Annelieke M. Roest, Erick H. Turner i Peter de Jonge. "Hiding negative trials by pooling them: a secondary analysis of pooled-trials publication bias in FDA-registered antidepressant trials". Psychological Medicine 49, nr 12 (28.09.2018): 2020–26. http://dx.doi.org/10.1017/s0033291718002805.
Pełny tekst źródłaKim, Daniel J., Dan Otap, Nora Ruel, Naveen Gupta, Naveed Khan i Tanya Dorff. "NCI–Clinical Trial Accrual in a Community Network Affiliated with a Designated Cancer Center". Journal of Clinical Medicine 9, nr 6 (24.06.2020): 1970. http://dx.doi.org/10.3390/jcm9061970.
Pełny tekst źródłaFoster, Henry H. "TRIAL MARRIAGES AND DIVORCE TRIALS". Family Court Review 11, nr 1 (15.03.2005): 1–7. http://dx.doi.org/10.1111/j.174-1617.1973.tb01183.x.
Pełny tekst źródłaHarman, Chloë. "Putting clinical trials on trial". Nature Reviews Nephrology 5, nr 6 (czerwiec 2009): 301. http://dx.doi.org/10.1038/nrneph.2009.89.
Pełny tekst źródłaMIZUSHIMA, YUTAKA. "New trials of trial cases." Rinsho yakuri/Japanese Journal of Clinical Pharmacology and Therapeutics 29, nr 1/2 (1998): 1–6. http://dx.doi.org/10.3999/jscpt.29.1.
Pełny tekst źródłaRozprawy doktorskie na temat "Trials"
Kim, Anne(Anne Y. ). "Optimizing clinical trials with Open Trial Chain". Thesis, Massachusetts Institute of Technology, 2018. https://hdl.handle.net/1721.1/121787.
Pełny tekst źródłaCataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 59-64).
The objective of this thesis is to study the challenges of data sharing in healthcare (namely clinical trials), and propose the use of Open Algorithms (OPAL) as a viable solution for research collaboration that allows for access to data without compromising data ownership (data is only used once for the intended purpose, raw data is never leaked, the value generated from the data is transferred to the owner). This thesis surveys the challenges unique to clinical trials, and highlights the various methods for privacy-preserving computation prior to this work. Through the overview of OPAL's solution in the space of privacy-preserving computation, we show the implementation details of how OPAL was applied to clinical trials in a project called Open Trial Chain, a platform for clinical trial data built for analytics, security, and incentivized sharing through technologies like federated learning and blockchain. With motivated examples derived from real-world reported problems in healthcare, we also demonstrate speed, accuracy, and security metrics. In the application, Open Trial Chain can drastically reduce clinical trial costs, reduce error, and increase quality of analysis diversity. Overall, this project shows promise for further extension in other health datasets for compliance in an ever-complicated move towards regulations that reflect for conscientiousness for data security, ownership, and provenance.
by Anne Kim.
M. Eng.
M.Eng. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science
Richert, Laura. "Trial design and analysis of endpoints in HIV vaccine trials". Thesis, Bordeaux 2, 2013. http://www.theses.fr/2013BOR22048/document.
Pełny tekst źródłaComplex data are frequently recored in recent clinical trials and require the use of appropriate statistical methods. HIV vaccine research is an example of a domaine with complex data and a lack of validated endpoints for early-stage clinical trials. This thesis concerns methodological research with regards to the design and analysis aspects of HIV vaccine trials, in particular the definition of immunogenicity endpoints and phase I-II trial designs. Using cytokine multiplex data, we illustrate the methodological aspects specific to a given assay technique. We then propose endpoint definitions and statistical methods appropriate for the analysis of multidimensional immunogenicity data. We show in particular the value of non-parametric multivariate scores, which allow for summarizing information across different immunogenicity markers and for making statistical comparisons between and within groups. In the aim of contributing to the design of new vaccine trials, we present the construction of an optimized early-stage HIV vaccine design. Combining phase I and II assessments, the proposed design allows for accelerating the clinical development of several vaccine strategies in parallel. The integration of a stopping rule is proposed from both a frequentist and a Bayesian perspective. The methods advocated in this thesis are transposable to other research domains with complex data, such as imaging data or trials of other immune therapies
Cuevas, Arriagada Ricardo Enrique, i Bustos Neil William Páez. "B-TRIALS". Tesis, Universidad de Chile, 2017. http://repositorio.uchile.cl/handle/2250/146375.
Pełny tekst źródłaRicardo Enrique Cuevas Arriagada [Parte I], Neil William Páez Bustos [Parte II]
El presente trabajo desarrolla una idea de negocio llamada B-Trials, cuyo origen surge a partir de una necesidad específica en la ejecución de Estudios Clínicos de la Industria Farmacéutica local, que corresponde al aumento en la participación de pacientes en la ejecución de los protocolos de estudios, a modo de aumentar la competitividad frente a los otros países de la región. Actualmente, son los médicos tratantes, colegas y/o contactos de los mismos quienes derivan pacientes a los Estudios Clínicos, por lo que este proyecto plantea la creación de una nueva forma de captación de pacientes e implementar una nueva forma de derivación de pacientes, con el fin de revolucionar a este mercado de USD $30 MM anuales. Gracias a la fluidez de los procesos regulatorios y obtención de resultados requeridos por las compañías farmacéuticas, es que Chile se hace atractivo, sopesando la menor cantidad de pacientes que puede ofrecer a diferencia de países como Argentina, Brasil, Colombia y México. Dado que desde los inicios de la Investigación Clínica en Chile se ha utilizado el mismo sistema de derivación de pacientes, B-Trials toma esta oportunidad y captará pacientes en el mundo de las Redes Sociales, que cada vez son más utilizadas por la sociedad, los que serán registrados en una página web y se construirá una base de datos propia. La base de datos permitirá identificar a distintos pacientes dispuestos a participar en los Estudios Clínicos, de acuerdo a parámetros clínicos específicos y zonas geográficas donde se encuentran, permitiendo la derivación de estos a Centros de Estudios ya operativos y dando la opción de tener la información necesaria para la instalación de un Centro de Estudios Clínicos propio en la ubicación con mayor demanda de pacientes y abastecerlo de pacientes. El equipo gestor está encargados del marketing, operaciones y comercial, áreas cruciales para la obtención de la ventaja competitiva. El proyecto B-Trials requiere de una Inversión Inicial de CLP $67 MM., con Payback de 3,5 años, TIR = 31% y VAN al año 5 de CLP $ 23 MM. Valor Residual = $ 403 MM. Tasa de descuento aplicada = 20,4%. B-Trials representa un negocio que satisface una necesidad de la Industria en forma innovadora, siendo pionero en el país y escalable en el territorio nacional y latinoamericano, mejorando la calidad de vida de los pacientes a través del acceso gratuito a tratamientos de última generación.
Dias, Claire Rhiannon. "Olympic trials". Thesis, Bangor University, 2014. https://research.bangor.ac.uk/portal/en/theses/olympic-trials(feb17a88-72fb-4577-9369-810a7420399e).html.
Pełny tekst źródłaLoudon, Kirstine. "PRECIS-2 : making trials matter : providing an empirical basis for the selection of pragmatic design choices in clinical trials". Thesis, University of Dundee, 2015. https://discovery.dundee.ac.uk/en/studentTheses/af271d88-4652-41e0-b280-4772cc30f8c4.
Pełny tekst źródłaCarvajal, Luis A. Rodriguez. "Multivariate crossover trials". Thesis, University of Warwick, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336783.
Pełny tekst źródłaKopec, David M., i Jeffrey J. Gilbert. "Overseeding Fairway Trials". College of Agriculture and Life Sciences, University of Arizona (Tucson, AZ), 2001. http://hdl.handle.net/10150/216378.
Pełny tekst źródłaBartoszuk, Karin. "Randomized Control Trials". Digital Commons @ East Tennessee State University, 2017. https://dc.etsu.edu/etsu-works/4161.
Pełny tekst źródłaJulian, Robert F. "The role of the judge and jury in complex trials". Thesis, Queen Mary, University of London, 2008. http://qmro.qmul.ac.uk/xmlui/handle/123456789/28172.
Pełny tekst źródłaCaldwell, Patrina Ha Yuen. "The Recruitment of Children to Randomised Controlled Trials". University of Sydney. Paediatrics and Child Health, 2003. http://hdl.handle.net/2123/579.
Pełny tekst źródłaKsiążki na temat "Trials"
Trial techniques and trials. New York: Wolters Kluwer Law & Business, 2013.
Znajdź pełny tekst źródłaMichael, Phillips, Bergman Barbara i Oregon Criminal Defense Lawyers Association., red. Trials and tribulations: (overcoming trial problems). Eugene, Or: [Oregon Criminal Defense Lawyers Association], 1999.
Znajdź pełny tekst źródłaTrials. New York, N.Y., U.S.A: Dutton, 1996.
Znajdź pełny tekst źródłaMerrill, Umphrey Martha, red. Trials. Aldershot, England: Ashgate, 2008.
Znajdź pełny tekst źródłaRafael, Nieves, Hayden Seitu i Baroza Aldin, red. Trials. San Jose, CA: SLG Pub., 1996.
Znajdź pełny tekst źródłaWallach, Anne Tolstoi. Trials. New York, N.Y., U.S.A: Dutton, 1996.
Znajdź pełny tekst źródłaMerrill, Umphrey Martha, red. Trials. Aldershot, England: Ashgate, 2008.
Znajdź pełny tekst źródłaMaxine, Caron, i Williams Wyn, red. Schools on trial: The trials of democratic comprehensives. Milton Keynes, England: Open University Press, 1985.
Znajdź pełny tekst źródłaFletcher, Colin. Schools on trial: The trials of democratic comprehensives. Milton Keynes: Open University Press, 1985.
Znajdź pełny tekst źródłaKlonoff, Robert H. Winning jury trials: Trial tactics and sponsorship strategies. Wyd. 3. Louisville, Colo: National Institute for Trial Advocacy, 2007.
Znajdź pełny tekst źródłaCzęści książek na temat "Trials"
Patra, Jayanta Kumar, Swagat Kumar Das, Gitishree Das i Hrudayanath Thatoi. "Clinical Trials". W A Practical Guide to Pharmacological Biotechnology, 109–26. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6355-9_6.
Pełny tekst źródłaBasu, Bikramjit, i Sourabh Ghosh. "Clinical Trials". W Biomaterials for Musculoskeletal Regeneration, 191–216. Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-3017-8_9.
Pełny tekst źródłaBlacher, Lynette, i Linda Marillo. "International Trials". W Principles and Practice of Clinical Trials, 1–22. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-52677-5_44-1.
Pełny tekst źródłaProrok, Philip C. "Screening Trials". W Principles and Practice of Clinical Trials, 1–19. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-52677-5_95-1.
Pełny tekst źródłaMcKneally, M. F., B. McPeek, F. Mosteller i E. A. M. Neugebauer. "Clinical Trials". W Surgical Research, 197–209. New York, NY: Springer New York, 1998. http://dx.doi.org/10.1007/978-1-4612-1888-3_26.
Pełny tekst źródłaRhoads, Kim F., i Julio E. Garcia-Aguilar. "Clinical Trials". W Transanal Endoscopic Microsurgery, 125–33. New York, NY: Springer New York, 2008. http://dx.doi.org/10.1007/978-0-387-76397-2_13.
Pełny tekst źródłaStaquet, M. "Clinical Trials". W Surgical Oncology, 446–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-72646-0_43.
Pełny tekst źródłaFriedman, Lawrence M., Curt D. Furberg i David L. DeMets. "Multicenter Trials". W Fundamentals of Clinical Trials, 427–40. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-1586-3_20.
Pełny tekst źródłaChen, Donna T. "Clinical Trials". W Encyclopedia of Women’s Health, 271–73. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-0-306-48113-0_91.
Pełny tekst źródłaCheng, Zhaoqi. "The Trials". W A History of War Crimes Trials in Post 1945 Asia-Pacific, 71–103. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6697-0_3.
Pełny tekst źródłaStreszczenia konferencji na temat "Trials"
Stubberfield, J. "ADSL trials". W IEE Seminar How Big is Your Pipe? Fast SoHo SME/Connectivity. IEE, 1999. http://dx.doi.org/10.1049/ic:19990322.
Pełny tekst źródłaKennedy, J., N. Sponagle, D. Wheaton, P. MacDonald i R. Creaser. "Video Systems For Propeller Viewing Trials". W SNAME 22nd American Towing Tank Conference. SNAME, 1989. http://dx.doi.org/10.5957/attc-1989-024.
Pełny tekst źródłaRelton, Clare. "Randomised Controlled Trials". W HRI London 2019—Cutting Edge Research in Homeopathy: Presentation Abstracts. The Faculty of Homeopathy, 2020. http://dx.doi.org/10.1055/s-0040-1702078.
Pełny tekst źródłaAnderson, James, Sarah Watts, Nigel Hills i Emmanuel Ofosu-Apeasah. "Submarine Towing Trials". W Warship 2005: Naval Submarines 8. RINA, 2005. http://dx.doi.org/10.3940/rina.ws.2005.17.
Pełny tekst źródłaThatcher, K. C., B. Grant i S. E. Welford. "RNLI Anchor Trials". W Surveillance, Pilot and Rescue Craft For The 21st Century. RINA, 1990. http://dx.doi.org/10.3940/rina.sur.1990.3.2.
Pełny tekst źródłaMartin, John R. "RISTA II trials". W SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, redaktorzy Wallace G. Fishell, Arthur A. Andraitis, Michael S. Fagan, Jerry D. Greer i Mark C. Norton. SPIE, 1998. http://dx.doi.org/10.1117/12.330204.
Pełny tekst źródłaRodriguez, M. B., P. Plaza i M. Ibanez. "ePerSpace Intemediate Trials". W International conference on Networking and Services (ICNS'06). IEEE, 2006. http://dx.doi.org/10.1109/icns.2006.46.
Pełny tekst źródłaHilsenbeck, S., i M. Piccart. "Clinical Trials 102: New Strategies in Targeted Therapy Clinical Trials." W Abstracts: Thirty-Second Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 10‐13, 2009; San Antonio, TX. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.sabcs-09-es5-1.
Pełny tekst źródłaPile, J. H. "Color Line “Superspeed 1” Trials 2009. The 1st Safeguard Trials". W Safeguard Passenger Evacuation Seminar. RINA, 2012. http://dx.doi.org/10.3940/rina.safe.2012.01.
Pełny tekst źródłaLetourneau, J. E. "Effect of the warning signal on visual reaction time during recovery from general anesthesia". W OSA Annual Meeting. Washington, D.C.: Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.tuy25.
Pełny tekst źródłaRaporty organizacyjne na temat "Trials"
Kaplan, Celia P. Minorities in Clinical Trials: Patients, Physicians, Clinical Trial Characteristics, and Their Environment. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2010. http://dx.doi.org/10.21236/ada542448.
Pełny tekst źródłaKaplan, Celia. Minorities and Clinical Trials: Patients, Physicians, Clinical Trial Characteristics, and Their Environment. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2011. http://dx.doi.org/10.21236/ada573587.
Pełny tekst źródłaKaplan, Celia P. Minorities and Clinical Trials: Patients, Physicians, Clinical Trial Characteristics and their Environment. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2012. http://dx.doi.org/10.21236/ada586285.
Pełny tekst źródłaNelson, Eric. First Trials with EMPHASIS. Office of Scientific and Technical Information (OSTI), wrzesień 2020. http://dx.doi.org/10.2172/1660566.
Pełny tekst źródłaFawcett, Jim, Zack Koopman, Wayne Roush i Josh Sievers. On-Farm Corn Rootworm Trials. Ames: Iowa State University, Digital Repository, 2015. http://dx.doi.org/10.31274/farmprogressreports-180814-1053.
Pełny tekst źródłaFawcett, Jim, Lance Miller, Lyle Rossiter, Wayne Roush, Josh Sievers, Micah Smidt i Matt Schnabel. On-Farm Soybean Fungicide Trials. Ames: Iowa State University, Digital Repository, 2015. http://dx.doi.org/10.31274/farmprogressreports-180814-1121.
Pełny tekst źródłaFawcett, Jim, Lance Miller, Lyle Rossiter, Wayne Roush, Josh Sievers, Micah Smidt i Matt Schnabel. On-Farm Soybean Fungicide Trials. Ames: Iowa State University, Digital Repository, 2015. http://dx.doi.org/10.31274/farmprogressreports-180814-1212.
Pełny tekst źródłaFawcett, Jim, Zack Koopman, Wayne Roush i Josh Sievers. On-Farm Corn Rootworm Trials. Ames: Iowa State University, Digital Repository, 2015. http://dx.doi.org/10.31274/farmprogressreports-180814-1261.
Pełny tekst źródłaFawcett, Jim, i Josh Sievers. On-Farm Corn Planter Trials. Ames: Iowa State University, Digital Repository, 2016. http://dx.doi.org/10.31274/farmprogressreports-180814-1408.
Pełny tekst źródłaFawcett, Jim, Josh Sievers i Lyle Rossiter. On-Farm Cover Crop Trials. Ames: Iowa State University, Digital Repository, 2016. http://dx.doi.org/10.31274/farmprogressreports-180814-1469.
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