A French Multicenter Observational Retrospective Study of Rare Primary Liver Cancers
NCT ID: NCT06541652
Last Updated: 2025-08-05
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.
RECRUITING
150 participants
OBSERVATIONAL
2024-03-26
2031-02-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
National Registry of Hepatic Metastases From Non-Colorectal Cancer"
NCT07180641
Next Generation Sequencing in Intrahepatic Cholangiocarcinoma
NCT02184871
Biliary Cancer in Italy: a Study on Cholangiocarcinoma cAUSEs and Risk Factors
NCT02665494
A Retrospective Review of Malignant Liver Tumors
NCT00728650
French Childhood Cancer Survivor Study
NCT01620372
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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
OTHER
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* with histologically proven hepato-cholangiocarcinoma, fibrolamellar hepatocellular carcinoma, epithelioid hemangioendothelioma or hepatic angiosarcoma
* diagnosed after January 01, 2018 living or deceased at the time of registration in the cohort
* for living patients who have not objected to the research: (note of non-objection to be attached° agreeing to participate in ancillary studies must sign the biological consent form for participation in biological studies.
Exclusion Criteria
* No access to tumor block
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Société Nationale Française de Gastroentérologie
OTHER
Federation Francophone de Cancerologie Digestive
OTHER
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.
jean-charles nault, Pr
Role: PRINCIPAL_INVESTIGATOR
Federation Francophone de Cancerologie Digestive
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU Amiens picardie
Amiens, , France
Chu Angers
Angers, , France
Ch - Centresimone Veil de Beauvais
Beauvais, , France
Chu Jean Minjoz
Besançon, , France
Ch Bethune Beuvry
Béthune, , France
Avicenne
Bobigny, , France
Cote de Nacre
Caen, , France
Centre Hospitalier
Calais, , France
Chu de Clichy Hopital Beaujon
Clichy, , France
Centre Hospitalier Universitaire Henri Mondor
Créteil, , France
CHU
Dijon, , France
Chu Grenobles Alpes
La Tronche, , France
Centre Hospital Universitaire de lille
Lille, , France
Longjumeau Ch Nord Essone
Longjumeau, , France
Ch Edouard Herriot
Lyon, , France
Centre Léon Berard
Lyon, , France
La Clinique de La Sauvegarde
Lyon, , France
Chu Edouard Herriot
Lyon, , France
Lyon Cac Leon Berard
Lyon, , France
Lyon La Croix Rousse
Lyon, , France
Hopital Saint Joseph
Marseille, , France
Chu de La Timone
Marseille, , France
CHR - Metz Thionville Hopital de Mercy
Metz, , France
CHU La Source
Orléans, , France
Chu de Paris Saint Antoine
Paris, , France
AP - HP - Pitié Salpêtrière
Paris, , France
PAU CH
Pau, , France
Centre Hospitalier de Perpignan
Perpignan, , France
Hopital Haut Leveque
Pessac, , France
Chu de Poitiers
Poitiers, , France
CH - Annecy Genevois
Pringy, , France
Chu Robert Debre
Reims, , France
CAC - Eugène Marquis
Rennes, , France
Ico Site Rene Gauducheau
Saint-Herblain, , France
Hopital Nord Chu Saint Etienne
Saint-Priest-en-Jarez, , France
Groupe Hospitalier Rance Emeraude
St-Malo, , France
Chu Rangueil
Toulouse, , France
Chru de Tours
Tours, , France
Chu Paul Brousse
Villejuif, , France
Gustave Roussy
Villejuif, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023-A01517-38
Identifier Type: REGISTRY
Identifier Source: secondary_id
CAPRIH COHORT
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.