Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID04006951

Development of a Clinical and Biological Database in Rectal Cancer to Support Research and Treatment

Led by Institut du Cancer de Montpellier - Val d'Aurelle · Updated on 2025-02-13

300

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to create a clinical and biological database focused on rectal cancer, a subtype of colorectal cancer that represents 40% of cases. Rectal cancer has significant challenges including controlling the cancer locally and generally, and managing treatment side effects. Currently, pre-operative radiochemotherapy combined with surgery is the standard care, but this approach often leads to postoperative complications and poor functional outcomes. The study focuses on improving knowledge about rectal cancer by collecting clinical data and biological samples to assist future research and treatment development. Participants in the study will provide paraffin tissue samples from pre-treatment rectal biopsies when applicable, and blood samples collected at multiple times: before any treatment and, if pre-operative radiochemotherapy is given, before surgery. Alongside this biological collection, standardized clinical data will be entered into a database. This initiative is led by the Montpellier Cancer Institute to support research on predictive markers for treatment response and disease recurrence. Participants will be involved over a period lasting up to 66 months, during which their consent rates will be tracked. The study collects tissue and blood samples to help develop new biomarkers and improve diagnostic and follow-up tests. No investigational treatments are given as part of this study. The research is observational with no blinding and includes adults aged 18 and older who receive care at the Montpellier Cancer Institute. Safety and compliance to study procedures are monitored throughout the participation.

CONDITIONS

Brief Title

Development of a Clinical and Biological Database in Rectum Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient treated at the Montpellier Cancer Institute, regardless of treatment type
  • Age over 18 years
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Not affiliated with the Social Protection system
  • Unable to understand or comply with study requirements due to psychological, family, social, or geographical reasons
  • Currently under legal guardianship

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Biological Sample Collection

Duration - Up to 66 months

Participants provide biological samples including blood and tissue samples before treatment and, if applicable, before surgery after pre-operative radiochemotherapy.

Samples collected at multiple time points before treatment and before surgery

Trial Site Locations

Total: 1 location

1

ICM Val d'Aurelle

Montpellier, France, 34298

Actively Recruiting

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Research Team

A

Aurore MOUSSION

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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Published Research Related To This Trial