Identifying risk factors for gallbladder cancer and gallstone disease
Establishment and Exploitation of a European-Latin American Research Consortium Towards Eradication of Preventable Gallbladder Cancer - EULAT Eradicate GBC
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 |
|---|---|
| Enrollment | 15000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Paul Strauss Academic / other |
| Locations | 36 sites (Salta and 35 other locations) |
| Trial ID | NCT06192719 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates include men and women aged 18 or over with gallbladder cancer, dysplasia, or scheduled for cholecystectomy due to gallstones.
Not a fit: Patients with medical or psychiatric conditions that interfere with informed consent or pose unreasonable risks will not benefit from this study.
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 performed: While there have been studies focusing on gallbladder cancer, this approach of integrating multifactorial risk assessments and creating a biorepository is relatively novel.
Eligibility criteria
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 this trial is running
Salta and 35 other locations
- 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)
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.