NCT06128343

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
107mo left

Started Nov 2023

Longer than P75 for all trials

Geographic Reach
1 country

8 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress22%
Nov 2023Feb 2035

First Submitted

Initial submission to the registry

November 7, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 13, 2023

Completed
3 days until next milestone

Study Start

First participant enrolled

November 16, 2023

Completed
11.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2035

Expected
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2035

Last Updated

March 19, 2026

Status Verified

March 1, 2026

Enrollment Period

11.2 years

First QC Date

November 7, 2023

Last Update Submit

March 16, 2026

Conditions

Keywords

Adenocarcinomafine-needle aspirationendoscopic ultrasonographyepidemiologybiobankDNA tumors

Outcome Measures

Primary Outcomes (1)

  • Enrichment of prospective BACAP collection

    This collection is coming to enrich the prospective BACAP collection of fresh tumor tissue and/or fixed from the micro-biopsy under endoscopic ultrasound

    5 years

Interventions

Collection of biological samples including whole blood and micro-biopsy from tissue of pancreas

Eligibility Criteria

Age18 Years - 120 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with a pancreatic adenocarcinoma proven cytologically or histologically without any treatment

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (8)

Béthune hospital center

Béthune, 62408, France

NOT YET RECRUITING

Haut-Lévêque Hospital

Bordeaux, 33604, France

NOT YET RECRUITING

Huriez Hospital

Lille, 59037, France

NOT YET RECRUITING

Jean Mermoz private hosptila

Lyon, 69008, France

NOT YET RECRUITING

Saint Eloi Hospital

Montpellier, 34295, France

NOT YET RECRUITING

Regional Cancer Center From Montpellier

Montpellier, 34298, France

NOT YET RECRUITING

PAU hospital

Pau, 6400, France

NOT YET RECRUITING

Rangueil hospital

Toulouse, 31059, France

RECRUITING

Related Publications (1)

  • Bardol T, Dujon AM, Taly V, Dunyach-Remy C, Lavigne JP, Costa-Silva B, Kurma K, Eslami-S Z, Cayrefourcq L, Canivet C, Muscari F, Bournet B, Alix-Panabieres C. Early detection of pancreatic cancer by liquid biopsy "PANLIPSY": a french nation-wide study project. BMC Cancer. 2024 Jun 10;24(1):709. doi: 10.1186/s12885-024-12463-8.

Biospecimen

Retention: SAMPLES WITH DNA

blood sample and micro-biopsy

MeSH Terms

Conditions

AdenocarcinomaCarcinomaNeoplasms

Condition Hierarchy (Ancestors)

Neoplasms, Glandular and EpithelialNeoplasms by Histologic Type

Study Officials

  • Barbara BOURNET, MD, PhD

    University Hospital, Toulouse

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Barbara BOURNET, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 7, 2023

First Posted

November 13, 2023

Study Start

November 16, 2023

Primary Completion (Estimated)

January 31, 2035

Study Completion (Estimated)

February 28, 2035

Last Updated

March 19, 2026

Record last verified: 2026-03

Locations