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Recruiting NCT06128343

NCT06128343 Anatomical-Clinical Base of Adenocarcinoma Pancreatic

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Clinical Trial Summary
NCT ID NCT06128343
Status Recruiting
Phase
Sponsor University Hospital, Toulouse
Condition Adenocarcinoma
Study Type OBSERVATIONAL
Enrollment 1,500 participants
Start Date 2023-11-16
Primary Completion 2035-01-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 120 Years
Study Type OBSERVATIONAL
Interventions
collection of biological samples

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 1,500 participants in total. It began in 2023-11-16 with a primary completion date of 2035-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

BACAP-2 is a prospective biobank dedicated to the pancreatic adenocarcinoma including clinical data and biological samples from tumor. The aim is to enrich the previous propective collection BACAP in order to support future research projects.

Eligibility Criteria

Inclusion Criteria: * Patient with pancreatic mass syndrome explored by ultrasound endoscopy with cytopuncture or * 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 or * Patient with pancreatic adenocarcinoma proven histologically and/or cytologically Exclusion Criteria: * Patient with a pancreatic tumor whose analysis histological is not an adenocarcinoma * Pregnant or breastfeeding patient

Contact & Investigator

Central Contact

Barbara BOURNET, MD, PhD

✉ bournet.b@chu-toulouse.fr

📞 (0)5 61 32 32 35

Principal Investigator

Barbara BOURNET, MD, PhD

PRINCIPAL INVESTIGATOR

University Hospital, Toulouse

Frequently Asked Questions

Who can join the NCT06128343 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 120 Years, studying Adenocarcinoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06128343 currently recruiting?

Yes, NCT06128343 is actively recruiting participants. Contact the research team at bournet.b@chu-toulouse.fr for enrollment information.

Where is the NCT06128343 trial being conducted?

This trial is being conducted at Béthune, France, Bordeaux, France, Lille, France, Lyon, France and 4 additional locations.

Who is sponsoring the NCT06128343 clinical trial?

NCT06128343 is sponsored by University Hospital, Toulouse. The principal investigator is Barbara BOURNET, MD, PhD at University Hospital, Toulouse. The trial plans to enroll 1,500 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology