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Preoperative Fasting vs. Not Fasting in Critically Ill Patients

Abroad (travel likely)Recruiting

Conditions

Critical Illness · Surgical Procedure, Unspecified · Pulmonary Aspiration · Fasting

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

  • Stanford Medical Center, Palo Alto, California, United States

    Contact: Study coordinator (Pedro Tanaka, MD, PhD, MACM) · ptanaka@stanford.edu · (650) 498-6000

  • UCSF Medical Center Parnassus, San Francisco, California, United States

    Contact: Study coordinator (Lee-lynn Chen, MD) · Lee-lynn.Chen@ucsf.edu · (415) 567-6600

  • University of Colorado Medical Center, Aurora, Colorado, United States

    Contact: Study coordinator (Ana Fernandez-Bustamante, MD, PhD, FASA) · 720-848-0000

  • University of Miami Hospital, Miami, Florida, United States

    Contact: Study coordinator (Alexander Fort III, MD) · acfort@med.miami.edu · 305-243-4000

  • McGaw Medical Center of Northwestern, Chicago, Illinois, United States

    Contact: Study coordinator (Ravindra Gupta, MD, FASA, FCCP) · Ravindra.Gupta@nm.org · (312) 503-7975

  • Rush University Medical Center, Chicago, Illinois, United States

    Contact: Study coordinator (Alisha Sachdev, MD) · Alisha_Sachdev@rush.edu · (888) 352-7874

  • University of Maryland Medical Center, Baltimore, Maryland, United States

    Contact: Study coordinator (Megan Anders, MD) · manders@som.umaryland.edu · (410) 328-8600

  • Mass General Hospital, Boston, Massachusetts, United States

    Contact: Study coordinator (Alex Nagrebetsky)

  • Brigham & Women's Hospital, Boston, Massachusetts, United States

    Contact: Study coordinator (Gyorgy Frendl)

  • University of Massachusetts Memorial Medical Center, Worcester, Massachusetts, United States

    Contact: Study coordinator (Guido Musch, MD, MBA) · Guido.Musch@umassmed.edu · (508) 334-1000

  • University of Minnesota Medical Center, Minneapolis, Minnesota, United States

    Contact: Study coordinator (Benjamin Keith, MD) · keith200@umn.edu · 855-324-7843

  • Columbia University Irvine Medical Center, New York, New York, United States

    Contact: Study coordinator (Vivek Moitra, MD, FASA, FCCP) · vm2161@cumc.columbia.edu · (212) 305-2500

  • Memorial Sloan Kettering Cancer Center, New York, New York, United States

    Contact: Study coordinator (David Amar, MD) · amard@mskcc.org · 212-639-2000

  • University of Rochester Medical Center, Rochester, New York, United States

    Contact: Study coordinator (Jacob Nadler, MD, PhD, FASA) · Jacob_Nadler@URMC.Rochester.edu · (585) 275-2100

  • Montefiore Medical Center, The Bronx, New York, United States

    Contact: Study coordinator (Michael Kiyatkin, MD) · mkiyatkin@montefiore.org · 718-920-4321

  • Wake Forest University Health Sciences, Winston-Salem, North Carolina, United States

    Contact: Study coordinator (Ashish Khanna, MD, FCCP, FCCM) · akhanna@wakehealth.edu · 336-758-5000

  • Cleveland Clinic, Cleveland, Ohio, United States

  • University of Texas Medical Branch, Galveston, Texas, United States

    Contact: Study coordinator (Marcos Vidal Melo, MD, PhD) · mfvidalm@UTMB.EDU · 409-772-1011

  • UT Health Houston, Houston, Texas, United States

    Contact: Study coordinator (Turan Mehmet, MD) · mehmet.a.turan@uth.tmc.edu · 713-486-1000
Study leads

  • Alexander Nagrebetsky, MD, MSC

    Principal Investigator

    Massachusetts General Hospital

View source on ClinicalTrials.gov(opens in a new tab)