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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03976960
Other study ID # BCB2014/01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 19, 2018
Est. completion date December 2030

Study information

Verified date August 2021
Source Institut du Cancer de Montpellier - Val d'Aurelle
Contact Jean-Pierre BLEUSE, M.D
Phone 4 67 61 31 02
Email DRCI-icm105@icm.unicancer.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Developement of a clinical and biological database in colon cancer and colic tumors in order to better understand tumor invasion and metastatic scattering processes. The investigators hope that a better understanding of tumoral invasion process will lead to the discovery of new biomarkers and new drugs.


Description:

As the second leading cause of cancer-related death in France, colorectal cancer is a major public health problem. Each year, 37 000 cases are newly diagnosed in France and 17 000 patients die of the disease. Colorectal cancer is due to molecular and genetic damages involved in all tumorigenesis steps, transition from healthy tissue to adenoma and finally to invasive carcinoma stage. The investigators hope that a to better understand tumor invasion and metastatic scattering processes will allow therapeutic innovation and the emergence of new biomarkers. However, the study of early tumorigenesis phases as well as advanced stages of the disease is currently limited due to a lack of tissue samples. In this context, the Montpellier Cancer Institute (ICM) decided to initiate a biological collection dedicated to the tissular and blood samples of patients with colorectal cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date December 2030
Est. primary completion date December 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patient undergoing colon cancer surgery (stage I, II, III and IV) 2. Patient operated for liver or lung or peritoneal carcinomatosis metastases originating from colon cancer 3. Patient operated for pre-neoplastic lesion (adenomatous polyp /villous adenoma polyp), 4. Patient with familial polyposis eligible for colectomy 5. Age > 18 years 6. Signed informed consent Exclusion Criteria: 1. Patient not affiliated to Social Protection system 2. Patient unable to understand or comply with study instructions or requirements for psychological, family, social or geographical reasons 3. Patient under guardianship 4. Minor patient

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Biological collection
The biological collection will also include samples of blood samples collected before or after surgery but also samples frozen and/or paraffin-embedded tissue sections.

Locations

Country Name City State
France CHRU de Montpellier Montpellier Hérault
France Institut Régional du cancer de Montpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
Institut du Cancer de Montpellier - Val d'Aurelle

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of clinical risk factors for colorectal cancer Until the study completion : 6 years
Primary Number of biological risk factors for colorectal cancer Until the study completion : 6 years
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