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  2. Newly Published Data Indicates St. Jude Medical Trifecta ...

    www.aol.com/news/2013-03-19-newly-published-data...

    Conducted at 31 medical centers in the U.S., Canada and Europe, the study followed 1,014 eligible patients implanted with the Trifecta valve between 2007 and 2009 as part of a U.S. Food and Drug ...

  3. ClinicalTrials.gov - Wikipedia

    en.wikipedia.org/wiki/ClinicalTrials.gov

    If the trial terminates for some reason (e.g., lack of enrollment, evidence of initial adverse outcomes), the status may be updated to 'terminated'. Once final trial results are known or legal deadlines are met, the trial record manager may upload basic summary results to the registry either by filling a complex web-based form or submitting a ...

  4. Abbott's heart valve repair device gets FDA advisers' backing

    www.aol.com/news/abbotts-heart-valve-repair...

    Advisers to the U.S. Food and Drug Administration on Tuesday backed an approval for Abbott Laboratories' heart valve repair device that is designed for patients who are at risk of complications or ...

  5. JANUS clinical trial data repository - Wikipedia

    en.wikipedia.org/wiki/JANUS_clinical_trial_data...

    Janus clinical trial data repository is a clinical trial data repository (or data warehouse) standard as sanctioned by the U.S. Food and Drug Administration (FDA). It was named for the Roman god Janus (mythology) , who had two faces, one that could see in the past and one that could see in the future.

  6. Abbott's heart valve repair device gains US FDA approval - AOL

    www.aol.com/news/abbotts-heart-valve-repair...

    (Reuters) -Abbott Laboratories said on Tuesday the U.S. FDA has approved its heart valve repair device for patients with a potentially fatal heart disease, just months after rival Edwards ...

  7. Case report form - Wikipedia

    en.wikipedia.org/wiki/Case_report_form

    The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient. All data on each patient participating in a clinical trial are held and/or documented in the CRF, including adverse events. The sponsor of the clinical trial develops the CRF to collect the specific data they need in order ...

  8. Transcatheter aortic valve replacement - Wikipedia

    en.wikipedia.org/wiki/Transcatheter_aortic_valve...

    The devices are implanted without open heart surgery. The valve delivery system is inserted in the body, the valve is positioned and then implanted inside the diseased aortic valve, and then the delivery system is removed. The catheter-based delivery system can be inserted into the body from one of several sites. [14]

  9. US FDA mandates label updates on CAR-T cancer therapies - AOL

    www.aol.com/news/us-fda-mandates-label-updates...

    The health regulor has required related updates to other sections of the label such as warnings and precautions, postmarketing experience, patient counseling information and medication guide. In ...