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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04637048
Other study ID # Obs-Hepatobiliary CA
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date February 16, 2017
Est. completion date December 1, 2023

Study information

Verified date June 2022
Source First Affiliated Hospital of Wenzhou Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Hepatobiliary tumors have a poor prognosis and high individual heterogeneity, the patient with hepatobiliary tumors even accepted radical surgery, the postoperative recurrence rate is still high. Therefore, it is of great significance to find important prognostic markers to improve patient prognosis and formulate new treatment plans. In recent years, targeted therapy and immunotherapy make cancer treatment enter a new field, However, tumor heterogeneity is the greatest challenge in cancer therapeutics and biomarkers discovery. In this study, we collected a wide rang of patients' information, including photos of patients' face, physical strength and nutrition indicators, blood ,stool and pathological tissue specimens from tumor patients, then Multi-omics testing were applied to Looking for novel therapeutic targets and prognostic markers to predict patient response to treatment. Clinicians choose the best treatment plan for the patient based on the test results to improve the patient's survival time and quality of life.


Description:

This is an ongoing, longitudinal, observational clinical cohort study of patients with tumors of the alimentary tract, mainly hepatobiliary tumors. All the patients are diagnosed, treated and followed up. In the future, some other patient information will be gradually updated to this database


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 1000
Est. completion date December 1, 2023
Est. primary completion date December 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Be older than 18 years old; 2. Clinical or pathological diagnosis of malignant hepatobiliary tumors; 3. Patients have received or are about to receive surgery, chemotherapy radiotherapy, targeted therapy, local therapy, immunotherapy, etc; 4. Patients understand and are willing to sign written informed consent. Exclusion Criteria: 1. Patients considered by the doctor to be unsuitable for entry into this study (mental disorder or poor compliance, etc.); 2. The patient or guardian is unwilling to participate in this study; 3. Pregnant women; 4. Combined with other serious systemic diseases (heart failure, renal failure,hematopoietic system disease or Uncontrollable acute infection); 5. Estimated survival time is less than 1 month.

Study Design


Locations

Country Name City State
China Gang Chen Wenzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Gang Chen, MD

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate the overall survival rate of all patients with hepatobiliary tumor In order to identify the potential influence factors of hepatobiliary tumor patients survival 5 years
Secondary Evaluate the recurrence free survival rate of patients with hepatobiliary tumor In order to identify the potential influence factors of tumor recurrencesamples from patients with hepatobiliary cancers 5 years
Secondary Evaluate the cancer-specific survival rate of patients with hepatobiliary tumor In order to identify the potential influence factors of tumor-induced death in patients with hepatobiliary tumors 5 years
Secondary Evaluate the Progression Free Survival rate of patients with hepatobiliary tumor In order to identify the potential influence factors of tumor progression from patients with hepatobiliary cancers 5 years
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