DILIN - Prospective Study

Part of paid clinical trials in Los Angeles, California.

Sponsor
Duke University
Study ID
NCT00345930
Status
Recruiting

Conditions

  • Liver Diseases

Eligibility Criteria

Sex
ALL
Age
2 Years - N/A
Healthy Volunteers
Accepted

Study Details

The purpose of this study is to identify individuals who have suffered a liver injury arising as an idiosyncratic reaction to a prescription drug or a complementary and alternative medicine. Recently added acute cases enrollment that meets criteria to the protocol. Also added Fibroscans to the protocol that will be completed at baseline and follow-up on chronic subjects.

Key Dates

Start date
Sep 30, 2004
Status verified
Apr 2026
Primary completion
Jul 31, 2028
Completion
Jul 31, 2028

Study Design

Enrollment
4,000 participants (estimated)

Arms

  • Arm: 2
    Individuals without drug induced liver disease
  • Arm: 1
    Individuals with drug induced liver disease

Primary Outcome Measure

Develop a database of recent DILI cases [ Time Frame: July 2028 ]

Central Contacts

Locations (6)

FacilityCityStateZIPSite coordinators
University of Southern CaliforniaLos AngelesCalifornia90033
Susan Milstein, RN, BSN
323-224-5441
Andrew Stolz, MD (PRINCIPAL_INVESTIGATOR)
Indiana UniversityIndianapolisIndiana46202-5111
Jennifer Terrell
317-278-6266
Naga P Chalasani, MD (PRINCIPAL_INVESTIGATOR)
NIH Clinical SiteBethesdaMaryland20892
Jaha nor
301-435-6122
Christopher Koh, MD (PRINCIPAL_INVESTIGATOR)
University of MichiganAnn ArborMichigan48109-0362
Josefa Kaganove
Robert J Fontana, MD (PRINCIPAL_INVESTIGATOR)
Univeristy of North Carolina at Chapel HillChapel HillNorth Carolina27599-7600
Jacquee Simpson
None Available
Paul B Watkins, MD (PRINCIPAL_INVESTIGATOR)
Thomas JeffersonPhiladelphiaPennsylvania19141
Katrin Koy
215-456-2004
Dina Halegoua-DeMarzio, MD (PRINCIPAL_INVESTIGATOR)

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