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Active, not recruiting No phase listed Observational

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

ClinicalTrials.gov ID: NCT03973372

Public ClinicalTrials.gov record NCT03973372. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 4:11 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Advancing Liver Therapeutic Approaches (ALTA). The ALTA Consortium Study Group for the Management of Portal Hypertension - A 5-year Longitudinal Observational Study of Patients Undergoing Transjugular Intrahepatic Portosystemic Shunt (TIPS) Placement

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03973372
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Enrollment
852 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 10, 2019 (Actual)
Primary completion
Dec 2026 (Estimated)
Completion
Dec 2027 (Estimated)
Last update posted
Feb 10, 2026

2019 – 2027

United States locations

U.S. sites
14
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
University of Arizona Phoenix Arizona 85006 —
Stanford Redwood City California 94063 —
Scripps Health San Diego California 92121 —
University of California San Francisco San Francisco California 94115 —
University of Florida Gainesville Florida 32608 —
Northwestern Chicago Illinois 60611 —
University of Chicago Chicago Illinois 60637 —
University of Minnesota Minneapolis Minnesota 55455 —
Mayo Clinic Rochester Rochester Minnesota 55905 —
Columbia University New York New York 10032 —
Weill Cornell New York New York 10065 —
Baylor Scott & White Liver Consultants of Texas Dallas Texas 75246 —
University of Texas Southwestern Medical Center Dallas Texas 75390 —
University of Wisconsin Madison Madison Wisconsin 53705 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03973372, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 10, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03973372 live on ClinicalTrials.gov.

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