Identifying risk factors for gallbladder cancer and gallstone disease
Official title: Establishment and Exploitation of a European-Latin American Research Consortium Towards Eradication of Preventable Gallbladder Cancer - EULAT Eradicate GBC
Run by Centre Paul Strauss · NCT06192719 · Data updated 2026-11-12
This study is trying to find out what causes gallbladder cancer and gallstone disease by looking at different lifestyle and genetic factors to help with early detection and prevention.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 15000 (estimated) |
| Sponsor | Centre Paul Strauss Academic / other |
| Locations | 36 sites (Salta and 35 other locations) |
| Status | Recruiting |
| Started | December 1, 2019 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | February 18, 2026 |
| Trial ID | NCT06192719 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include men and women aged 18 or over with gallbladder cancer, dysplasia, or scheduled for cholecystectomy due to gallstones.
✕Probably not a fit
Patients with medical or psychiatric conditions that interfere with informed consent or pose unreasonable risks will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study focuses on gallbladder cancer (GBC) and gallstone disease, aiming to improve early detection and risk estimation for GBC. Researchers will analyze various epidemiological factors, including geographical, environmental, lifestyle, and genetic influences, to develop a multifactorial risk score. The study will also create a biorepository and an IT platform to facilitate the identification and validation of novel GBC biomarkers. By understanding the causal mechanisms linking lifestyle and GBC, the study seeks to enhance prevention strategies and guide clinical decisions regarding gallbladder removal.
Why it matters
Potential benefit: If successful, this study could lead to improved early detection and prevention strategies for gallbladder cancer, potentially saving lives.
How similar studies have gone: While there have been studies focusing on gallbladder cancer, this approach of integrating multifactorial risk assessments and creating a biorepository is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Cohort A. Patients with gallbladder cancer or dysplasia, both before and after the start of their anticancer treatment. Cohort B. Patients with cholelithiasis before cholecystectomy (only patients scheduled for cholecystectomy will be recruited) 2. Diagnosis confirmed in accordance with standard protocols of the participating hospitals 3. Men and women aged 18 or over Exclusion Criteria: 1. Any medical condition that present an unreasonable risk to the participant. 2. Any psychiatric condition that interferes with understanding informed consent.
Where it's running
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Hospital Papa Francisco
Salta, Argentina Recruiting -
Sanatorio el Carmen
Salta, Argentina Recruiting -
Hospital Pablo Soria
San Salvador de Jujuy, Argentina Recruiting -
Complejo Hospitalario Viedma
Cochabamba, Bolivia Recruiting -
Hospital del Norte
Cochabamba, Bolivia Recruiting -
Hospital Obrero No. 2 (Caja Nacional del Seguro Social)
Cochabamba, Bolivia Recruiting
Show 30 more locations
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Instituto Gastroenterológico
Cochabamba, Bolivia Recruiting -
Instituto Oncológico Nacional
Cochabamba, Bolivia Recruiting -
Hospital Regional de Arica
Arica, Chile Recruiting -
Hospital Regional de Concepción
Concepción, Chile Recruiting -
Hospital De Puerto Montt
Port Montt, Chile Recruiting -
Hospital Clínico de Magallanes
Punta Arenas, Chile Recruiting -
Hospital Regional de Rancagua
Rancagua, Chile Recruiting -
Clínica Alemana de Santiago
Santiago, Chile Recruiting -
Fundación Arturo López Perez (FALP)
Santiago, Chile Recruiting -
Hospital Barros Luco
Santiago, Chile Recruiting -
Hospital Clínico Universidad de Chile
Santiago, Chile Recruiting -
Hospital del Salvador
Santiago, Chile Recruiting -
Hospital El Pino
Santiago, Chile Recruiting -
Hospital Padre Hurtado
Santiago, Chile Recruiting -
Hospital San Borja
Santiago, Chile Recruiting -
Hospital San Juan de Dios
Santiago, Chile Recruiting -
Hospital Sótero del Río
Santiago, Chile Recruiting -
Hospital Regional de Talca
Talca, Chile Recruiting -
Clínica Alemana de Temuco
Temuco, Chile Recruiting -
Complejo Asistencial Padre Las Casas
Temuco, Chile Recruiting -
Hospital Regional de Temuco
Temuco, Chile Recruiting -
Centre Paul Strauss
Strasbourg, France Recruiting -
Hospital Goyoneche
Arequipa, Peru Recruiting -
Hospital Honorio Delgado
Arequipa, Peru Recruiting -
Instituto Regional de Enfermedades Neoplásicas del Sur (IREN Sur)
Arequipa, Peru Recruiting -
Clínica Monte Sinaí
Juliaca, Peru Recruiting -
Hospital Base III- La Capilla ESSALUD
Juliaca, Peru Recruiting -
Instituto Nacional de Enfermedades Neoplásicas (INEN)
Lima, Peru Recruiting -
Hospital Regional Manuel Nuñez Butrón
Puno, Peru Recruiting -
Instituto Regional de Enfermedades Neoplásicas del Norte (IREN Norte)
Trujillo, Peru Recruiting
Study contacts
- Principal investigator: Justo LORENZO BERMEJO, PhD — Heidelberg University Hospital (UKHD, Germany) and Centre Paul Strauss (CPS, France)
- Study coordinator: Dominique SCHERER, PhD
- Email: scherer@imbi.uni-heidelberg.de
- Phone: +49 6221 56 7303
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.