NCT07587216

Brief Summary

This study is a prospective, observational, real-world cohort study. We aim to establish a prospective database in the Department of Hepatobiliary and Pancreatic Surgery, systematically collecting and integrating patients' full-course diagnostic and therapeutic information along with long-term outcomes. This will enable objective evaluation of prognosis and treatment efficacy in real-world clinical practice, while providing a data foundation and evidence support for subsequent optimization of clinical decision-makin

Trial Health

77
On Track

Trial Health Score

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

Enrollment
800

participants targeted

Target at P75+ for all trials

Timeline
44mo left

Started Jan 2026

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress10%
Jan 2026Dec 2029

Study Start

First participant enrolled

January 1, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

May 8, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 14, 2026

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2029

Last Updated

May 14, 2026

Status Verified

May 1, 2026

Enrollment Period

2 years

First QC Date

May 8, 2026

Last Update Submit

May 8, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • overall survival

    From date of treatment until the date of death from any cause, assessed up to 100 months

Secondary Outcomes (1)

  • Incidence of Adverse Events

    Within 30 days following interventions

Study Arms (2)

Liver resection group

Procedure: liver resection

Non-surgery group

Drug: Systemic therapy combined with locoregional interventions

Interventions

Patients undergo liver resection for tumor.

Liver resection group

Patients recieve PD-1 inhibitors combined with targeted drugs and locoregional interventions

Non-surgery group

Eligibility Criteria

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

patients with liver cancer

You may qualify if:

  • Male or female aged ≥18 years at the time of signing the informed consent form;
  • Clinically or histologically confirmed diagnosis of liver cancer;
  • Recieving treatment and follow-up in Tongji Hospital

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, 430030, China

RECRUITING

MeSH Terms

Conditions

Liver NeoplasmsNeoplasm Metastasis

Interventions

Hepatectomy

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesLiver DiseasesNeoplastic ProcessesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Digestive System Surgical ProceduresSurgical Procedures, Operative

Central Study Contacts

Qi Cheng, M.D.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
2 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Deputy Director of Hepatobiliary and Pancreatic Surgery Department

Study Record Dates

First Submitted

May 8, 2026

First Posted

May 14, 2026

Study Start

January 1, 2026

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2029

Last Updated

May 14, 2026

Record last verified: 2026-05

Locations