PPT-Should I Enroll in a Clinical Trial?

Author : tatyana-admore | Published Date : 2017-08-26

David N Assis MD Assistant Professor of Medicine Yale University I have no disclosures relevant to this presentation Clinical Trials in PSC PSC is a rare disease

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Should I Enroll in a Clinical Trial?: Transcript


David N Assis MD Assistant Professor of Medicine Yale University I have no disclosures relevant to this presentation Clinical Trials in PSC PSC is a rare disease 32000 patients in the US PSC has no proven and approved treatment. ucscedu 3 Click Enroll 2 Click Main Menu then My Student Center folder then My St udent Center page yp e in the 5 digit class number or find a clas s by conducting a Class Search Click Enter 4 If there is more than one quarter available s elect the AMWA Northern California Chapter . 04 Oct 2014. 10/4/2014. 1. Topics. Relevant definitions, background. Protocol audiences. Purposes of protocols. Protocol components. Per ICH . E6 . Additional (synopsis, glossary, appendices). help users enroll in the wireless network. Such a solutionis painful and hardly practical even in a well-supportedenterprise setting, making it completely infeasible force networks.User-friendly PKI d Eugene Yang, MD, FACC. Clinical Associate Professor of Medicine. Medical Director, UW Medicine Eastside Specialty Center. University of Washington School of Medicine. UW MEDICINE . | . WA ACC CVT PROGRAM 2016. in the On - Site on JAG University 1. Go to JAG University at: https://jagu.army.mil/ 2. Log in using either your CAC, or your AKO user name and password. 3. Upon logging in, you’ll be taken to the x0000x0000 x/Attxachexd /xBottxom x/BBoxx 7x2 21x036x 75 x368x04 x/Subxtypex /Foxoterx /Tyxpe /xPagixnatixon 0x/Attxachexd /xBottxom x/BBoxx 7x2 21x036x 75 x368x04 x/Subxtypex /Foxoterx /Tyxpe /xPagix Barry R. Davis, MD, PhD. University of Texas School of Public Health. Houston, TX. Duke Industry Statistics Symposium . A. re Pragmatic Trials Ready for Prime Time?. September 7, 2017. Outline. Description of . Unblinding. and Termination. Within-trial . decisions . are decisions that need to be made once a . clinical trial.  has already . started, . for example, if there is an . unexpected . problem. . These . T. he . trial sponsor . compiles . a detailed clinical study report (CSR. ) after each clinical trial. . This report follows . a format laid down by the regulatory . authorities.. The CSR can be hundreds of pages long.. “Putting it All Together. ”. 1. Why the changes to NIH-funded studies involving human subjects?. No policies existed to make sure that the public had access to results from unpublished NIH-funded research . Collecting data. 2. Data . Statistics is a way of thinking—thinking about ways to . gather. and analyze data.. Trust data. 3. 3. Resource of Data. Experiment/ clinical trial. Survey. http://www.nhs.uk/Conditions/Clinical-trials/Pages/Healthresearch.aspx. PERFUSE Medical Research &. Clinical Trial Course. Clara Fitzgerald, MPH. The Importance of Clinical Trial Protocols. The Clinical Trial Protocol is the complete written description of, and scientific rational for clinical research studies. Conducting a Clinical Trial. Wendy M Kohrt, PhD. Nancy Anschutz Chair in Women’s Health Research. Distinguished Professor of Medicine, Division of Geriatric Medicine. University of Colorado – Anschutz Medical Campus. B. rain . I. njury . T. reatment Trial: A Multicenter Phase II Adaptive Clinical Trial. . Gaylan. . Rockswold. , MD, PhD, Principal Investigator. Thomas Bergman, MD, Site Principal Investigator. Overview.

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