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Spots Global Cancer Trial Database for Direct Acting Antiviral-Post Authorization Safety Study

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Trial Identification

Brief Title: Direct Acting Antiviral-Post Authorization Safety Study

Official Title: DAA-PASS: A Post-Authorisation Safety Study of Early Recurrence of Hepatocellular Carcinoma in HCV-Infected Patients After Direct-Acting Antiviral Therapy

Study ID: NCT03707080

Interventions

Study Description

Brief Summary: This is an independent optional sub-study parallel to TARGET-HCC (NCT02954094). The purpose of Direct-Acting Antiviral-Post Authorization Safety Study (DAA-PASS) is to investigate the impact of exposure to direct-acting antivirals (DAAs) on early recurrence of hepatocellular carcinoma (HCC) in hepatitis C virus (HCV)-infected patients following successful HCC treatment interventions.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Banner University Medical Center, Phoenix, Arizona, United States

University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

Norris Comprehensive Cancer Center, Los Angeles, California, United States

Stanford University, Palo Alto, California, United States

California Liver Research Institute, Pasadena, California, United States

University of California - Davis Clinical Trials, Sacramento, California, United States

University of California - San Francisco, San Francisco, California, United States

Georgetown University, Washington, District of Columbia, United States

Gastro Florida, Clearwater, Florida, United States

University of Florida Hepatology Research at CTRB, Gainesville, Florida, United States

University of Florida - Health Gastroenerology, Jacksonville, Florida, United States

Schiff Center for Liver Diseases, Miami, Florida, United States

Tampa General Medical Group, Tampa, Florida, United States

Piedmont Atlanta Hospital, Atlanta, Georgia, United States

Emory University Hospital, Atlanta, Georgia, United States

Northwestern University Division of Gastroenterology and Hepatology, Chicago, Illinois, United States

Rush University Medical Center, Chicago, Illinois, United States

University of Iowa Hospitals and Clinics, Iowa City, Iowa, United States

Tulane University School of Medicine, New Orleans, Louisiana, United States

Mercy Medical Center, Baltimore, Maryland, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

University of Michigan, Ann Arbor, Michigan, United States

Henry Ford Health System, Detroit, Michigan, United States

Mayo Clinic, Rochester, Minnesota, United States

Southern Therapy and Advanced Research LLC, Jackson, Mississippi, United States

Saint Louis University, Saint Louis, Missouri, United States

Rutgers-Robert Wood Johnson Medical School, New Brunswick, New Jersey, United States

Northwell Health - Center for Liver Disease, Manhasset, New York, United States

New York University Langone Health, New York, New York, United States

Weill Cornell Medical College, New York, New York, United States

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

Carolinas HealthCare System Center for Liver Disease, Charlotte, North Carolina, United States

Providence Health & Services Cancer Clinical Trials, Portland, Oregon, United States

Penn State Hershey Medical Center, Hershey, Pennsylvania, United States

University of Pennsylvania, Philadelphia, Pennsylvania, United States

Medical University of South Carolina, Charleston, South Carolina, United States

Vanderbilt University Medical Center - GI Research Office, Nashville, Tennessee, United States

Clinical Research Institute@ Methodist Dallas Medical Center, Dallas, Texas, United States

University of Texas Southwestern Medical Center, Dallas, Texas, United States

Baylor Scott & White All Saints, Fort Worth, Texas, United States

Research Specialists of Texas, Houston, Texas, United States

Research Specialists of Texas, Houston, Texas, United States

University of Virginia Transplant Center, Charlottesville, Virginia, United States

Bon Secours Liver Institute of Virginia, Richmond, Virginia, United States

Virginia Commonwealth University, Richmond, Virginia, United States

Harborview Medical Center, Seattle, Washington, United States

Wenatchee Valley Hospital & Clinics, Wenatchee, Washington, United States

CHU de Nice - HĂ´pital L'Archet 2, Nice, , France

HĂ´pitaux Universitaires Paris Centre, Paris, , France

CharitÊ - Universitätsmedizin Berlin, Berlin, , Germany

Universitätsklinikum Frankfurt, Frankfurt, , Germany

Universitätsklinikum Leipzig, Leipzig, , Germany

Universitätsklinikum Magdeburg, Magdeburg, , Germany

Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, , Italy

A.O.U.P. di Palermo, Palermo, , Italy

Humanitas Mirasole IRCCS, Rozzano, , Italy

IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo, , Italy

Hospital Puerta de Hierro Majadahonda, Madrid, , Spain

ClĂ­nica Universidad de Navarra, Pamplona, , Spain

Hospital Universitario Marques de Valdecilla, Santander, , Spain

Hospital Universitario Virgen del RocĂ­o, Sevilla, , Spain

Hospital Universitario Politècnic La Fe, Valencia, , Spain

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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