Actively Recruiting
Development of a Monocentric and Prospective Clinical and Biological Database in Digestive Cancers, Gynecological Cancers, Breast Cancers and Sarcomas
Led by Institut du Cancer de Montpellier - Val d'Aurelle · Updated on 2025-02-12
4000
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are developing a comprehensive clinical and biological database focused on various types of cancer, including digestive, gynecologic, breast cancers, and sarcomas. This database supports research in epidemiology, biology, and clinical trials by helping scientists understand tumor behavior, from molecular interactions to metabolism in healthy and diseased states. It aims to identify new strategies for cancer prevention, diagnosis, and treatment by providing reliable clinical and biological data. The study collects biological samples such as frozen tumor and healthy tissues during surgery and blood samples taken at different times for diagnostic and treatment purposes, including additional samples for research. Alongside this biological collection, standardized clinical data are systematically entered into a database. This integrated approach facilitates multidisciplinary research, harmonizing data collection and sharing to support medical progress and the identification of molecular markers. Participants are patients aged 18 or older with confirmed or suspected invasive or in situ tumors of digestive, gynecologic, breast, or sarcoma cancers, who have not yet received treatment and require tumor surgery. Researchers measure the proportion of patients consenting to participate over about one year. The study involves ongoing assessments through biological samples and clinical data collection, enabling long-term research and monitoring to enhance understanding and innovation in cancer care.
CONDITIONS
Brief Title
Development of Clinical and Biological Database
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Patient with invasive or in situ tumor pathology (proven or suspected) at any stage
- Diagnosis at Institut du Cancer de Montpellier of digestive cancer (esophagus, stomach, pancreas, colon, rectum, anal canal), gynecologic cancer (ovary, endometrium, cervix), breast cancer, or sarcoma
- No prior treatment for the current cancer
- Patient requires at least one tumor surgery
- Patient agrees to provide supplementary blood samples
- Patient has given informed, written, and express consent
You will not qualify if you...
- Not affiliated with a social protection scheme
- Regular follow-up unlikely due to psychological, familial, social, or geographical reasons
- Pregnant or nursing women
- Subject under tutelage, curatorship, or safeguard of justice
- Patient in an emergency situation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo tumor surgery during which tissue samples (tumor and healthy tissue) are collected and preserved for research.
1 visit (in-person)
Duration - Throughout diagnosis and treatment period
Participants provide blood samples at various times during diagnosis and treatment for research purposes alongside routine clinical blood draws.
Blood samples collected during routine clinical visits
Duration - Ongoing during participant involvement
Standardized clinical data are collected and entered into a database in parallel with biological sample collection to support research.
Data collected during routine healthcare visits
Trial Site Locations
Total: 1 location
1
Institut regional du Cancer - Val d Aurelle
Montpellier, France, 34298
Actively Recruiting
Research Team
D
david azria
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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