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NCT03978078Recruiting

A Clinicobiological Database in Metastatic Digestive Cancers

Development of a Prospective Clinicobiological Database in Metastatic Digestive Cancers

Source: ClinicalTrials.gov · Last updated 12 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Creation of a collection of blood samples that will be collected before and then under treatment in patients with digestive adenocarcinoma during the 1st and 2nd metastatic line and which, depending on scientific progress, can be used for research projects aimed at developing tailored patient management strategies.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
5 Jun 2019
Start date
12 Sept 2016
Primary completion date
Sept 2026
Lead sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
NCT number
NCT03978078

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 12 Sept 2016 to the primary completion date, Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient already undergoing specific treatment (chemotherapy and/or targeted therapy) in 1st or 2nd metastatic line

Age

  • Male or female \< 18 years old

Other

  • Non-adenocarcinoma histological type
  • Pregnant and/or breastfeeding woman
  • Patient not affiliated to a social security system
  • Patient whose regular follow-up is impossible for psychological, family, social or geographical reasons
  • Patient who is included in a Phase I-II therapeutic trial modifying usual management and involving additional and specific blood samples

Who the study is looking for

  • Male or female ≥ 18 years old
  • Histological documentation of adenocarcinoma of the colon or rectum, small intestine, pancreas, stomach, bile duct, oesophagus
  • Patient who will receive a first or second line metastatic chemotherapy and/or targeted therapy
  • Informed consent form (ICF) signed

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Institut Regional Du Cancer de Montpellier
Coordinator of this site? Confirm its status
MontpellierFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.