LEADER 05321nam 2200637Ia 450 001 9910830835203321 005 20230828223721.0 010 $a1-280-44821-0 010 $a9786610448210 010 $a0-470-32719-7 010 $a0-471-93091-1 010 $a0-471-93087-3 035 $a(CKB)1000000000354555 035 $a(EBL)257228 035 $a(OCoLC)647776971 035 $a(SSID)ssj0000196687 035 $a(PQKBManifestationID)11172008 035 $a(PQKBTitleCode)TC0000196687 035 $a(PQKBWorkID)10154026 035 $a(PQKB)10267923 035 $a(MiAaPQ)EBC257228 035 $a(EXLCZ)991000000000354555 100 $a20051129d2006 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 12$aA manager's guide to the design and conduct of clinical trials$b[electronic resource] /$fPhillip I. Good 205 $a2nd ed. 210 $aHoboken, NJ $cWiley-Liss$dc2006 215 $a1 online resource (274 p.) 300 $aDescription based upon print version of record. 311 $a0-471-78870-8 320 $aIncludes bibliographical references and indexes. 327 $aA MANAGER'S GUIDE TO THE DESIGN AND CONDUCT OF CLINICAL TRIALS; Contents; 1 Cut Costs and Increase Profits; No Excuse for the Wastage; Front-Loaded Solution; Downsizing; Think Transnational; A Final Word; 2 Guidelines; Start with Your Reports; The Wrong Way; Keep It in the Computer; Don't Push the River; KISS; Plug the Holes as They Arise; Pay for Results, Not Intentions; Plan, Do, Then Check; PART I PLAN; 3 Prescription for Success; Plan; A. Predesign Phase; B. Design the Trials; Do; C. Obtain Regulatory Agency Approval for the Trials; D. Form the Implementation Team 327 $aE. Line Up Your Panel of PhysiciansF. Develop the Data Entry Software; G. Test the Software; H. Train; I. Recruit Patients; J. Set Up External Review Committees; K. Conduct the Trials; L. Develop Suite of Programs for Use in Data Analysis; M. Analyze and Interpret the Data; Check; N. Complete the Submission; 4 Staffing for Success; The People You Need; Design Team; Obtain Regulatory Approval for the Trials; Track Progress; Implementation Team; Develop Data Entry Software; Test the Software; Line Up Your Panel of Physicians; External Laboratories; Site Coordinators; External Review Committees 327 $aRecruit and Enroll PatientsTransnational Trials; Conduct the Trials; Programs for Data Analysis; Analyze and Interpret the Data; The People You Don't Need; For Further Information; 5 Design Decisions; Should the Study Be Performed?; Should the Trials Be Transnational?; Study Objectives; End Points; Secondary End Points; Should We Proceed with a Full-Scale Trial?; Tertiary End Points; Baseline Data; Who Will Collect the Data?; Quality Control; Study Population; Timing; Closure; Planned Closure; Unplanned Closure; Be Defensive. Review, Rewrite, Review Again; Checklist for Design 327 $aBudgets and ExpendituresFor Further Information; 6 Trial Design; Baseline Measurements; Controlled Randomized Clinical Trials; Randomized Trials; Blocked Randomization; Stratified Randomization; Single- vs. Double-Blind Studies; Allocation Concealment; Exceptions to the Rule; Sample Size; Which Formula?; Precision of Estimates; Bounding Type I and Type II Errors; Equivalence; Software; Subsamples; Loss Adjustment; Number of Treatment Sites; Alternate Designs; Taking Cost into Consideration; For Further Information; 7 Exception Handling; Patient Related; Missed Doses; Missed Appointments 327 $aNoncomplianceAdverse Reactions; Reporting Adverse Events; When Do You Crack the Code?; Investigator Related; Lagging Recruitment; Protocol Deviations; Site-Specific Problems; Closure; Intent to Treat; Is Your Planning Complete?; PART II DO; 8 Documentation; Guidelines; Common Technical Document; Reporting Adverse Events; Initial Submission to the Regulatory Agency; Sponsor Data; Justifying the Study; Objectives; Patient Selection; Treatment Plan; Outcome Measures and Evaluation; Procedures; Clinical Follow-Up; Adverse Events; Data Management, Monitoring, Quality Control; Statistical Analysis 327 $aInvestigator Responsibilities 330 $aThis newly updated edition of the benchmark guide to computer-assisted clinical trials provides a comprehensive primer for prospective managers. It covers every critical issue of the design and conduct of clinical trials, including study design, organization, regulatory agency liaison, data collection and analysis, as well as recruitment, software, monitoring, and reporting.Keeping the same user-friendly format as the original, this Second Edition features new examples and the latest developments in regulatory guidelines, such as e-submission procedures and computerized direct data acq 606 $aClinical trials 606 $aClinical medicine$xResearch 615 0$aClinical trials. 615 0$aClinical medicine$xResearch. 676 $a610.72/4 676 $a610.724 700 $aGood$b Phillip I$0102489 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830835203321 996 $aA manager's guide to the design and conduct of clinical trials$93964734 997 $aUNINA