ClinicalTrials.gg
Not yet recruitingNCT06276153CRGGCextUpdated Feb 28, 2024

Construction of Multicenter Retrospective Registry Cohort Database for Gallbladder Cancer

An observational study in Biliary Tract Diseases, Gallbladder Cancer and Gallbladder Neoplasms, sponsored by RenJi Hospital. Not yet recruiting. Open to participants aged 18 Years to 74 Years. Per ClinicalTrials.gov, last updated 2024-02-28.

Primary conditionGallbladder NeoplasmsRegistry: Biliary Tract DiseasesReclassifiedWhy we changed it
Registry
Biliary Tract Diseases — the first condition term the registry derived for this study.
ClinicalTrials.gg
Gallbladder Neoplasms
Why
  1. The study's listed conditions name Gallbladder Neoplasms, a narrower term within Biliary Tract Diseases.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by RenJi Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
5,000
Ages
18 Years to 74 Years
Sex
All
01

Study summary

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.

Read the detailed description

From the date of commencement of the study, patients who presented to the participating medical institutions in the study and were clinically diagnosed as gallbladder cancer, and who met the inclusion criteria and did not meet any of the exclusion criteria, were enrolled in the study cohort after signing an informed consent form.

The research objectives of this study mainly include establishing a structured dataset standard for gallbladder cancer based on the diagnosis and treatment norms and clinical pathways and carrying out clinical registration research on gallbladder cancer and build a specific disease cohort

The outcome indicators of this study included overall survival time OS, recurrence-free survival time PFS, R0 resection rate of patients treated with biliary malignancy, and objective response rate ORR. The main measurement indicators of this study include the patient's demographic information, past history, life history, admission, preoperative examination information, surgery, postoperative situation, discharge, follow-up, outcome indicators, routine examination results of biological samples and multi-omics sequencing results, the above data are derived from the original records of prospective case questionnaires, the original records of patients' electronic medical records and the examination results of patients' biological samples. The outcome of follow-up was defined as patients having been followed up for five years, or having a patient lost to follow-up or dying during follow-up.

02

Conditions studied

  • Biliary Tract Diseases
  • Gallbladder Cancer
  • Gallbladder Neoplasms

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Keywords

  • gallbladder cancer
  • gallbladder neoplasms
  • cohort study
  • registry cohort
  • biliary tract neoplasms
03

In context

Gallbladder Neoplasms Reclassified

301 studies on the registry are indexed under Gallbladder Neoplasms; 65 are open to participants now.

This study's planned enrollment of 5,000 is above the median of 200 across 61 observational studies indexed under Gallbladder Neoplasms.

Browse Gallbladder Neoplasms studies →

Lead sponsor

RenJi Hospital is the lead sponsor of 550 studies on the registry; 247 are open to participants now.

Compared within Gallbladder Neoplasms, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Biliary Tract Diseases. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years to 74 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with gallbladder cancer diagnosed by pathology, and combined with clinical manifestations and imaging results, the first diagnosis and discharge were diagnosed as patients with gallbladder cancer.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Sign , 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.
  • performance score greater than 50.

Exclusion criteria

Exclusion Criteria:

  • Patients with gallbladder cancer, gallbladder cancer foci are not primary lesions.
  • Patients with gallbladder cancer, combined with serious central nervous system diseases, respiratory diseases, diseases, chronic renal insufficiency and other diseases, long-term use of , 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 , 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.
  • The patient is participating in other therapeutic clinical trials where treatment measures cannot be clarified or treatment information cannot be collected .
Terms in these criteria, in plain language(5)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Karnofsky performance status (KPS)

A 0–100 scale of how well someone can carry out everyday activities. 100 is no complaints and no signs of illness; 70 is able to look after yourself but not to work or keep up normal activity; 50 is needing considerable help and frequent medical care.

Studies often ask for 60 or 70 and above. Your doctor gives the score.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
5,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Gallbladder cancer

    Diagnostic criteria: Patients with gallbladder cancer diagnosed by pathology, and combined with clinical manifestations and imaging results, the first diagnosis and discharge were diagnosed as patients with gallbladder cancer.

    Other: no interventions

Interventions

  • Otherno interventions

    retrospective registry cohort with no other specific interventions

06

What researchers measure

Primary outcomes

  1. overall survival

    OS in patients with biliary malignancies was long-term follow-up data, defined as the primary endpoint, OS is calculated from the date of surgery for patients treated surgically, and OS is calculated from the date of diagnosis for patients treated non-surgically. The expected survival of patients with benign biliary tumors is longer, and this study does not select the study endpoint based on the follow-up of patients with benign biliary tumors, but mainly collects perioperative diagnosis and treatment data and collects biological samples.

    Time frame: From date of enrollment until the date of death from any cause, whichever came first, assessed up to 5-years.

Secondary outcomes

  1. progression-free survival

    PFS was defined as a secondary endpoint. PFS is calculated from the date of surgery for patients treated surgically, and PFS is calculated from the date of diagnosis for patients treated non-surgically. The expected survival of patients with benign biliary tumors is longer, and this study does not select the study endpoint based on the follow-up of patients with benign biliary tumors, but mainly collects perioperative diagnosis and treatment data and collects biological samples.

    Time frame: From date of enrollment until the date of first documented progression from any cause, whichever came first, assessed up to 5-years.

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Mar 2024; primary completion for Feb 2027, 35 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 18, 2024
First posted
Feb 23, 2024
StartEst.
Mar 1, 2024
Primary completionEst.
Feb 28, 2027
CompletionEst.
Feb 28, 2029
Last update
Feb 28, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 28, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06276153
Lead sponsor
RenJi Hospital
Responsible party
Liu Ying-bin (Director of Pancreato-biliary Surgery, Principal Investigator, Professor, RenJi Hospital) — Principal investigator
First posted
Feb 23, 2024
Start date
Mar 1, 2024 (estimated)
Primary completion
Feb 28, 2027 (estimated)
Completion
Feb 28, 2029 (estimated)
Last update
Feb 28, 2024

Study contacts

Xu-Heng SUN, PhD.
Contact
sunxh96@sjtu.edu.cn
+8619117209107
Yi-Jun Wang, MD.
Contact
wangyijun1998@sjtu.edu.cn
+8618521757838
Ying-Bin Liu, PhD.
principal investigator · RenJi Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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