China Metastatic Liver Cancer Clinical Registry Cohort Database
1 other identifier
observational
2,000
1 country
3
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2026
Longer than P75 for all trials
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 16, 2026
CompletedFirst Posted
Study publicly available on registry
May 22, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
May 31, 2031
Study Completion
Last participant's last visit for all outcomes
May 31, 2036
May 22, 2026
May 1, 2026
5 years
May 16, 2026
May 16, 2026
Conditions
Keywords
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
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
The First Affiliated Hospital of USTC (Anhui Provincial Hospital)
Hefei, Anhui, 230001, China
The Affiliated Hospital of Qingdao University
Qingdao, Shandong, 266003, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
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