Construction of Multicenter Retrospective Registry Cohort Database for Gallbladder Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-74
SponsorRenJi Hospital

About this trial

The aim of the study is to establishing a standardized clinical information database for patients with malignant tumors of gallbaldder. Based on the database, real-world clinical research on the diagnosis and treatment of biliary tract tumors is about to be carried out, and a high-standard cohort research foundation is laid for precision therapy.

Eligibility criteria

Qualifiers

Sign informed consent, have good compliance, and be willing to accept follow-up and provide blood samples

Age 18-74 years old, gender is not limited

Clinical diagnosis of gallbladder cancer, including unoperated patients preliminarily diagnosed as gallbladder cancer according to the results of imaging examinations and laboratory tests, or pathological examination of patients treated with surgery confirmed as malignant tumors of the gallbladder.

The primary tumor is located in gallbladder floor, gallbladder body, gallbladder neck or gallbladder duct.

Disqualifiers

Patients with gallbladder cancer, gallbladder cancer foci are not primary lesions.

Patients with gallbladder cancer, combined with serious central nervous system diseases, respiratory diseases, autoimmune diseases, chronic renal insufficiency and other diseases, long-term use of immunosuppressants, combined with serious uncontrolled infections.

Patients with gallbladder cancer, who also have active cardiovascular and cerebrovascular diseases, have cerebrovascular accidents, myocardial infarction, unstable angina pectoris, or grade II. or above congestive heart failure according to the standards of the New York Heart Association, and require serious arrhythmias requiring drug treatment.

Patients with gallbladder cancer, women of childbearing age who have a positive blood pregnancy test or have not had a pregnancy test, pregnant or breastfeeding women.

Trial design

Treatments tested in this trial

  • no interventions

Treatment groups

5,000 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators