NCT07602504

Brief Summary

This study is led by the Department of Hepatobiliary Surgery of the First Affiliated Hospital of the University of Science and Technology of China (USTC), in close collaboration with multiple participating centers nationwide. The primary objective is to establish a standardized, large-scale clinical cohort database specifically for metastatic liver cancer. By collecting comprehensive data on patient demographics, primary tumor characteristics, systemic therapies, and local interventions, this registry aims to elucidate the clinical patterns and prognostic factors of secondary liver malignancies. This database will serve as a robust platform for conducting high-quality real-world studies and advancing evidence-based clinical research in the management of metastatic liver cancer.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
122mo left

Started Jun 2026

Longer than P75 for all trials

Geographic Reach
1 country

3 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 16, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 22, 2026

Completed
10 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Expected
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 31, 2031

5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2036

Last Updated

May 22, 2026

Status Verified

May 1, 2026

Enrollment Period

5 years

First QC Date

May 16, 2026

Last Update Submit

May 16, 2026

Conditions

Keywords

Liver Metastases; Metastatic Colorectal Cancer

Outcome Measures

Primary Outcomes (1)

  • Overall Survival

    The time interval from the date of initial diagnosis (or date of enrollment/surgery) to the date of death from any cause.

    Up to 10 years

Secondary Outcomes (2)

  • Progression-Free Survival

    Up to 10 years

  • Treatment-Related Adverse Events

    Within 90 days post-treatment

Interventions

In this observational patient registry, no specific interventional procedure is assigned by the investigators. Patients included in the database receive standard clinical management and treatments for metastatic liver cancer according to current clinical guidelines and physician's discretion. These procedures may include hepatectomy, ablation, transarterial chemoembolization (TACE), systemic chemotherapy, targeted therapy, or immunotherapy. This registry aims to evaluate the real-world effectiveness and safety of these standard interventions.

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

This registry targets adult patients with histologically or radiologically confirmed metastatic liver cancer. The population encompasses patients undergoing various standard clinical management strategies, including surgical resection, local ablation, transarterial chemoembolization (TACE), and systemic therapies (chemotherapy, targeted therapy, or immunotherapy).

You may qualify if:

  • Patients with histologically or radiologically confirmed metastatic liver cancer.
  • Age ≥ 18 years.
  • Patients who have voluntarily signed the informed consent form.
  • Patients with complete baseline clinical data.

You may not qualify if:

  • Patients with primary liver cancer (e.g., hepatocellular carcinoma).
  • Patients with other malignant tumors that may interfere with the evaluation of liver metastasis.
  • Patients who have previously participated in other interventional clinical trials.
  • Patients with severe cognitive disorders or communication barriers that prevent informed consent.
  • Patients with incomplete or missing key clinical data.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

The First Affiliated Hospital of Bengbu Medical University

Bengbu, Anhui, 230001, China

NOT YET RECRUITING

The First Affiliated Hospital of USTC (Anhui Provincial Hospital)

Hefei, Anhui, 230001, China

RECRUITING

The Affiliated Hospital of Qingdao University

Qingdao, Shandong, 266003, China

RECRUITING

MeSH Terms

Conditions

Liver NeoplasmsNeoplasmsLiver DiseasesColorectal Neoplasms

Interventions

Standard of Care

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesIntestinal NeoplasmsGastrointestinal NeoplasmsGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal Diseases

Intervention Hierarchy (Ancestors)

Quality Indicators, Health CareQuality of Health CareHealth Services AdministrationHealth Care Quality, Access, and Evaluation

Central Study Contacts

Jizhou Wang, MD PhD

CONTACT

Lianxin Liu, MD PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
10 Years
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 16, 2026

First Posted

May 22, 2026

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

May 31, 2031

Study Completion (Estimated)

May 31, 2036

Last Updated

May 22, 2026

Record last verified: 2026-05

Locations