Actively Recruiting

Age: 18Years - 120Years
All Genders
ID06128343

Anatomical-Clinical Base of Adenocarcinoma Pancreatic

Led by University Hospital, Toulouse · Updated on 2026-03-19

1500

Participants Needed

8

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pancreatic cancer is a leading cause of cancer death in Western countries, with over 90% of cases caused by adenocarcinoma. Surgical removal of the tumor is currently the only curative treatment but is possible in only 10 to 15% of cases. This research aims to enhance understanding and treatment of pancreatic adenocarcinoma by enriching an existing biobank with fresh tumor tissue and genetic analysis to support future studies on diagnostic tools, tumor development, therapeutic targets, and chemotherapy response.

CONDITIONS

Brief Title

Anatomical-Clinical Base of Adenocarcinoma Pancreatic

Who Can Participate

Age: 18Years - 120Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with pancreatic mass syndrome explored by ultrasound endoscopy with cytopuncture
  • Patient with pancreatic mass syndrome explored by an abdominal scanner with and without injection of product contrast and/or puncture of the mass or secondary lesions by radiological route
  • Patient with pancreatic adenocarcinoma proven histologically and/or cytologically
  • Age between 18 and 120 years
Not Eligible

You will not qualify if you...

  • Patient with a pancreatic tumor whose histological analysis is not an adenocarcinoma
  • Pregnant or breastfeeding patient

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 to 2 visits depending on diagnostic procedures

Diagnostic Evaluation

Duration - Up to 5 years

Participants undergo collection of biological samples including whole blood and micro-biopsy from pancreatic tissue to support research.

Visits occur as needed for sample collection during routine clinical care

Long-term Monitoring

Duration - Up to 5 years

Participants are observed over time to enrich the prospective BACAP collection and support future research.

Periodic visits may occur depending on clinical follow-up

Trial Site Locations

Total: 8 locations

1

Béthune hospital center

Béthune, France, 62408

Not Yet Recruiting

2

Haut-Lévêque Hospital

Bordeaux, France, 33604

Not Yet Recruiting

3

Huriez Hospital

Lille, France, 59037

Not Yet Recruiting

4

Jean Mermoz private hosptila

Lyon, France, 69008

Not Yet Recruiting

5

Saint Eloi Hospital

Montpellier, France, 34295

Not Yet Recruiting

6

Regional Cancer Center From Montpellier

Montpellier, France, 34298

Not Yet Recruiting

7

PAU hospital

Pau, France, 6400

Not Yet Recruiting

8

Rangueil hospital

Toulouse, France, 31059

Actively Recruiting

Loading map...

Research Team

B

Barbara BOURNET, MD, PhD

C

Cindy CANIVET, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Similar Trials

Usefulness of Tumor Heterogeneity Assessment in Patients Wit...

Prostatic Neoplasms

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial