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NCT06008548: PTA4HCC

A New Conception About Individualized Treatment Allocation for HCC

Completed Last updated 23 August 2023
What this trial tests

trial testing TACE in HCC in 4,991 participants. Completed in 1 October 2021.

Timeline
1 January 2010
Primary endpoint
30 January 2021
1 October 2021

Quick facts

Lead sponsorTang-Du Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment4,991
Start date1 January 2010
Primary completion30 January 2021
Estimated completion1 October 2021

Drugs / interventions tested

Conditions studied

Sponsor

Tang-Du Hospital

Who can join

Adults 18 to 100, any sex, with HCC or Transarterial Chemoembolization. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The current guidelines on hepatocellular carcinoma (HCC) aimed to build effective prognostic stratification strategies to guide therapeutic allocation; however, the current guidelines did not consider the simultaneous comparison of distinct therapies in similar populations. Here, the investigators aimed to develop and validate a new, integrated prognostic scheme for HCC patients using artificial intelligence (AI) to simulate the survival outcomes of patients allocated to different treatments.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of TACE

Trials testing the same drug.

Other recruiting trials for HCC

Currently open trials in the same condition.

Other Tang-Du Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06008548.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing