Status:

COMPLETED

Identify Proteomic Biomarkers for Outcome Prediction of Locoregional Treatments for HCC

Lead Sponsor:

University of Texas Southwestern Medical Center

Conditions:

Hepatocellular Carcinoma

Eligibility:

All Genders

18-70 years

Brief Summary

This study will enroll patients with hepatocellular carcinoma being planned for TACE or other standard of care treatment (such as denovo ablation or Y90) and obtain blood samples pre and post treatmen...

Detailed Description

This is a prospective, non-blinded, multi-arm study. Patients at 18 - 70 years old with liver cancer will be enrolled. The approach is to identify novel proteomic biomarkers for HCC patients treated ...

Eligibility Criteria

Inclusion

  • Ability to understand and the willingness to sign a written informed consent.
  • Male or female aged 18-70years.
  • Diagnosed with primary or metastatic liver cancer.
  • Scheduled to undergo Lipoidal TACE, denovo ablation, or Yttrium-90 (Y90) radioembolization as part of standard of care.

Exclusion

  • Subjects who have received chemotherapy, radiation or surgery for HCC.

Key Trial Info

Start Date :

November 4 2022

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 23 2025

Estimated Enrollment :

17 Patients enrolled

Trial Details

Trial ID

NCT04459468

Start Date

November 4 2022

End Date

September 23 2025

Last Update

January 8 2026

Active Locations (1)

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UT Southwestern Medical Center

Dallas, Texas, United States, 75390