Clinical trial Recruiting at 36 sites Observational Ages 18 and up

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 typeObservational
Ages18 Years and up
SexAll
Enrollment15000 (estimated)
SponsorCentre Paul Strauss
Academic / other
Locations36 sites (Salta and 35 other locations)
StatusRecruiting
StartedDecember 1, 2019
Main results expectedDecember 31, 2028
Study endsDecember 31, 2028
Registry record updatedFebruary 18, 2026
Trial IDNCT06192719 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

  • 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
  • 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

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.