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008 200310s2020 gw | o |||| 0|eng d
020 _a9783030354886
024 7 _a10.1007/978-3-030-35488-6
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
_dES-MaUEC
050 4 _aR853
_b.C55 2020 EB
245 0 0 _aClinical Trials
_cedited by Timothy M. Pawlik, Julie A. Sosa.
250 _aSecond edition 2020
264 1 _aCham
_bSpringer International Publishing :
_bImprint: Springer
_c2020.
300 _a1 recurso en línea (VI, 258 páginas)
_b26 ilustraciones, 16 ilustraciones a color
336 _2rdacontent
_aTexto
_btxt
337 _2rdamedia
_aelectrónico
_bc
338 _2rdacarrier
_arecurso electrónico
_bcr
347 _aArchivo de texto
_bPDF
490 0 _aSuccess in Academic Surgery
_x2194-7481
490 0 _aMedicine (Springer-11650)
505 0 _aHistory of Clinical Trials -- Ethics (COI, informed consent) -- Generating a Testable Hypothesis and Underlying Principles of Clinical Trials -- Trial Design: Overview of Study Designs (phase I, II, III, IV, factorial design) -- Defining the Study Cohort: Inclusion and Exclusion criteria (establishing eligibility and exclusion criteria, how should one define a cohort, balance between being inclusive versus selective / efficacy versus effectiveness trials) -- Building your Clinical Trial Research Team (how to assemble the team: database manager, research nurse) -- Clinical Trials: Ensuring Quality and Standardization (GCP, reporting of AE's, establishing SOPs, CRF's) -- Device versus Drug Clinical Trials: Similarities and Important Differences -- Statistics - Setting the Stage (Sample Size, Power, Randomization, Type II error, Treatment allocation/stratification) -- Statistics - Handling the Data (Intention to Treat analyses, Subgroups analyses, expressing the data (relative risk), handling missing data) -- Data Safety Monitoring Board: Interim Analyses, Stopping Rules -- Planning for Data Monitoring and Audit -- Clinical Trials: The Budget -- Regulatory Issues (compliance issues, IRB, FDA) -- Publishing your Clinical Trial (authorship, manuscript preparation, journal selection) -- Pragmatic clinical trials -- Cooperative trials -- International trials -- Inclusion of Patient Reported Outcomes -- Participation in clinical trials/as a clinical trialist for the community surgeon. .
520 3 _aThis extensively revised second edition is a unique and portable handbook focusing on clinical trials in surgery. It includes new educational materials addressing the rapid evolution of novel research methodologies in basic science, clinical and educational research. The underlying principles of clinical trials, trial design, the development of a study cohort, statistics, data safety, data monitoring, and trial publication for device and drug trials are also discussed. Clinical Trials provides a comprehensive resource on clinical trials in surgery and describes all the stages of a clinical trial from generating a hypothesis through to trial publication and is a valuable resource for all practicing and trainee academic surgeons.
650 7 _2embne
_9144524
_aEnsayos clínicos
700 1 _aPawlik, Timothy M.
_eeditor literario
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
_0http://id.loc.gov/authorities/names/nb2014002176
700 1 _aSosa, Julie A.
_eeditor literario
_4edt
_4http://id.loc.gov/vocabulary/relators/edt
710 2 _aSpringerLink (Online service)
_0http://id.loc.gov/authorities/names/no2005046756
773 0 _tSpringer eBooks
776 0 8 _iPrinted edition:
_z9783030354879
776 0 8 _iPrinted edition:
_z9783030354893
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-3-030-35488-6
_zAcceso a este recurso digital (usuarios Universidad Europea de Valencia)
942 _2lcc
_cLE
998 _db
_zSI