Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
4749 participants
OBSERVATIONAL
2017-01-11
2020-06-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The gallbladder is a small organ below the liver. Gallbladder cancer is a leading cause of cancer death among women in Chile. Chile also has among the highest rates of gallbladder cancer and death in the world. Researchers in a high-risk region of Chile want to find out more about this type of cancer. They especially want to know how inflammation affects the way it develops.
Objective:
To better understand the causes of gallbladder diseases and factors that may be associated with them.
Eligibility:
Women ages 50 74 with gallbladder cancer who are covered by the Chilean national health system.
Other people over age 21 with gallbladder disease.
Healthy adults over age 21.
Design:
Participants may be screened with an ultrasound. They may be asked questions about their health.
Participants will have an ultrasound of the abdomen. This can be done at the study clinic or in the hospital or at home. The ultrasound uses sound waves to take pictures of the gallbladder.
Participants will have a physical exam.
Participants will have their mouths looked at for tooth loss, dentures, and gum redness.
Participants will give a blood sample or saliva sample.
Participants will be asked for access to their medical history. They may be asked to allow researchers to keep any samples taken during gallbladder surgery.
Participants will answer questions about their medical history. This will include illnesses, surgeries, medicine use, and family history. It will also include diet and lifestyle habits, such as places where they have lived and worked.
Some participants will have 3 follow-up visits over 6 years.
...
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Pancreatico-biliary Tumor Mutation Profiling in Bile Samples
NCT02893085
Predicting Incidental Gallbladder Cancer
NCT06531408
Storage of Bile From Routine Procedures to Study Risk Factors
NCT00414843
EULAT Eradicate GBC
NCT06192719
Efficacy of Choleretics in Acalculous Gallbladder in Situ After Endoscopic Removal of Biliary Stones
NCT01829139
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
While the vast majority of gallbladder cancer cases have gallstones, only a small fraction of gallstone patients ever develop gallbladder cancer. Since there is no way to identify this small proportion at risk, gallstone cases are cholecystectomized, which, given large absolute numbers of individuals with gallstones, results in overtreatment of some and under-treatment of others in a high-risk area like Chile. While cholecystectomy is standard treatment for symptomatic relief, there are more people who need surgery than there are surgeons to perform them, and individuals aged 34-49 are prioritized for treatment, regardless of symptoms. This practice may lead to overtreatment among 34-49-year-olds and under treatment of individuals aged 50 and above since they have to wait longer for surgery. At the same time, about 30% of patients with a biliary colic attack will never have another attack, and cholecystectomy does not always lead to the cessation of symptoms. In addition, cholecystectomy has been associated with an increased risk of other digestive diseases. Thus, cholecystectomy may not be needed in all gallstone patients and may in fact increase the risk of cancer in some. Better predictors of risk are clearly needed.
As with other cancers, dysplasia is an important epidemiologic endpoint as the immediate precursor to cancer since the vast majority of gallbladder cancers develop through a histologic continuum of chronic cholecystitis, pseudopyloric metaplasia, incomplete intestinal metaplasia, dysplasia, and cancer. Thus, our aim is to identify risk factors for gallbladder dysplasia and cancer (GDC) and potential non-invasive risk stratification methods, such as ultrasound characteristics alone or in combination with inflammatory markers and patient characteristics, to better understand the etiology and natural history of GDC and to help inform strategies for GDC prevention.
Together with collaborators at Pontifica Universidad Catolica (PUC), we successfully completed a pilot study in Chile that was previously reviewed and approved by SAG and provided baseline data for the proposed study. Our pilot demonstrated high recruitment rates in the target enrollment area (80%) and high rates of questionnaire completion (100%), blood collection (78% population-based controls), and participant retention (93% of eligible completed a follow-up visit). Information from the pilot was used to optimize procedures for the longitudinal study. We also found that both gallstones and gallbladder cancer were associated with systemic immune alterations, which as we previously demonstrated, reflect inflammatory changes in the gallbladder detectable in bile. The next step is to demonstrate that these markers precede GDC by longitudinally measuring their levels among gallstone patients.
We propose to prospectively assess risk factors and early detection markers for GDC by conducting the Chile Biliary Longitudinal Study (BiLS), a cohort study of 6250 individuals with gallstones from the high- risk southern-central region of Chile. Because women are twice as likely to have gallstones and twice as likely to have gallbladder cancer as men, we plan to maximize our screening efficiency and number of outcomes by screening and enrolling women only. This approach is reasonable given that the female gender bias for gallbladder cancer is largely thought to be due to the gender bias for gallstones,1-3 suggesting that in the presence of gallstones, the risk of gallbladder cancer is the same for men and women. In addition, Chile is conducting a general population cohort in a small town in the high-risk area, and we can use the men with gallstones enrolled by the Chilean study to compare to the women in our study. We plan to enroll women with gallstones over 2 years and follow them for 6 years, conducting visits every other year to collect data on the primary exposures of interest, inflammatory markers and ultrasound characteristics, as well as additional exposures of interest, such as infections, genetics, and environmental exposures (e.g., aflatoxin, pesticides).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Women with gallstones
Women aged 50-74 with gallstones
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Female
* Age 50 years to 74 years
* No previous cholecystectomy
* Covered by National Health Insurance
* Resident of Araucania (or Maule)
* Able to answer questionnaire (due to language/communication issues or mental incapacity)
Other control (general population or cholecystectomy):
* No previous cholecystectomy
* Covered by National Health Insurance
* Resident of Araucania (or Maule)
* Able to answer questionnaire (due to language/communication issues or mental incapacity)
Gallbladder Cancer Group:
* Diagnosis within study time period
* Primary site of cancer is the gallbladder with histological or radiological confirmation
* Covered by National Health Insurance
* Resident of Araucania (or Maule)
* Able to answer questionnaire (due to language/communication issues or mental incapacity)
Exclusion Criteria
* Male
* Age less than 50 years or greater than 74 years
* History of previous cholecystectomy
* Not covered by National Health Insurance
* Not a Resident of Araucania (or Maule)
* Unable to answer questionnaire (due to language/communication issues or mental incapacity)
Other control (general population or cholecystectomy):
* History of previous cholecystectomy
* Not covered by National Health Insurance
* Not a Resident of Araucania (or Maule)
* Unable to answer questionnaire (due to language/communication issues or mental incapacity)
Gallbladder Cancer Group:
* Diagnosis not within study time period
* Primary site of cancer is NOT the gallbladder with histological or radiological confirmation
* Not covered by National Health Insurance
* Not a Resident of Araucania (or Maule)
* Unable to answer questionnaire (due to language/communication issues or mental incapacity)
50 Years
74 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Cancer Institute (NCI)
NIH
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jill E. Koshiol, M.D.
Role: PRINCIPAL_INVESTIGATOR
National Cancer Institute (NCI)
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hospital Regional de Talca
Talca, , Chile
Universidad Catolica del Maule
Talca, , Chile
Hospital Regional de Temuco
Temuco, , Chile
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
16-C-N070
Identifier Type: -
Identifier Source: secondary_id
999916070
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.