NCT05759858

Brief Summary

To explore the key genes of human and mouse hepatocellular carcinoma, identify the key genes and prognostic markers, and develop small molecule drugs targeting the key genes to treat hepatocellular carcinoma.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
unknown

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

Study Start

First participant enrolled

December 14, 2022

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

February 26, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

March 8, 2023

Completed
2.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

March 8, 2023

Status Verified

December 1, 2022

Enrollment Period

3 years

First QC Date

February 26, 2023

Last Update Submit

February 26, 2023

Conditions

Keywords

Hepatocellular carcinomaGenomesPrognosisGene targeted therapy

Outcome Measures

Primary Outcomes (3)

  • Key gene differences in hepatocellular carcinoma

    Key gene differences in hepatocellular carcinoma explored by RNA-seq.

    Through study completion, an average of 1 year.

  • Overall survival

    The time from the beginning of treatment to death (for any reason).

    Through study completion, up to 5 years.

  • Disease-free survival

    The time from the beginning of treatment to death (for any reason).

    Through study completion, up to 5 years.

Secondary Outcomes (1)

  • The incidence and mortality of postoperative hemorrhage, bile leakage and other complications.

    Through study completion, up to 5 years.

Study Arms (1)

Patients with hepatocellular carcinoma confirmed by pathology.

Patients with hepatocellular carcinoma confirmed by pathology.

Other: None of intervention

Interventions

None of the interventions was applied.

Patients with hepatocellular carcinoma confirmed by pathology.

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients suffered hepatocellular carcinoma which was confirmed by pathology. Only surgical treatment is applied to patients.

You may qualify if:

  • Hepatocellular carcinoma confirmed by pathology;
  • The patient has no combined organic diseases of heart, lung, and kidney, etc;
  • No history of chemotherapy, radiotherapy, upper abdominal surgery, or combined with other tumors;
  • The patient has successfully completed the operation and has complete clinical information and pathological data.

You may not qualify if:

  • Patients who have previous history of other tumors or have undergone upper abdominal surgery;
  • Patients with multiple lesions and distant metastasis;
  • Patients who are complicated with organic diseases of important organs such as heart, lung and kidney and cannot tolerate surgery;
  • Patients who are more than 75 years old or less than 18 years old.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

2nd Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, Zhejiang, China

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Samples were restored at -80℃ for 5 years.

MeSH Terms

Conditions

Carcinoma, Hepatocellular

Condition Hierarchy (Ancestors)

AdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsLiver NeoplasmsDigestive System NeoplasmsNeoplasms by SiteDigestive System DiseasesLiver Diseases

Study Officials

  • Sheng Yan, Doctor

    2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

    STUDY CHAIR
  • Yang Tian, Doctor

    2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

    STUDY DIRECTOR
  • Yuancong Jiang, Doctor

    2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sheng Yan, Doctor

CONTACT

Yang Tian, Doctor

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 26, 2023

First Posted

March 8, 2023

Study Start

December 14, 2022

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

March 8, 2023

Record last verified: 2022-12

Locations