ALTA TIPS: A 5-year Longitudinal Observational Study of Patients Undergoing TIPS Placement

NCT03973372 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 852

Last updated 2026-02-10

No results posted yet for this study

Summary

ALTA is a multicenter consortium focused on the management of portal hypertension. ALTA TIPS is a longitudinal observational study of patients who are undergoing transjugular intrahepatic portosystemic shunt (TIPS) placement. ALTA will create a database that will provide clinical parameters and outcomes of patients undergoing TIPS as part of their standard of care in hopes of answering key clinical questions.

Conditions

  • Cirrhosis, Liver
  • Transjugular Intrahepatic Portosystemic Shunt (TIPS)

Sponsors & Collaborators

  • University of California, San Francisco

    collaborator OTHER
  • Scripps Health

    collaborator OTHER
  • University of Wisconsin, Madison

    collaborator OTHER
  • University of Florida

    collaborator OTHER
  • University of Arizona

    collaborator OTHER
  • Stanford University

    collaborator OTHER
  • Columbia University

    collaborator OTHER
  • Weill Medical College of Cornell University

    collaborator OTHER
  • Baylor Scott and White Health

    collaborator OTHER
  • Mayo Clinic

    collaborator OTHER
  • University of Chicago

    collaborator OTHER
  • W.L.Gore & Associates

    collaborator INDUSTRY
  • University of Minnesota

    collaborator OTHER
  • Northwestern University

    collaborator OTHER
  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • Lisa VanWagner, MD · University of Texas Southwestern Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-06-10
Primary Completion
2026-12-31
Completion
2027-12-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03973372 on ClinicalTrials.gov