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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06128343
Other study ID # RC31/21/0191
Secondary ID 2021-A01050-41
Status Recruiting
Phase
First received
Last updated
Start date November 16, 2023
Est. completion date February 28, 2035

Study information

Verified date November 2023
Source University Hospital, Toulouse
Contact Barbara BOURNET, MD, PhD
Phone (0)5 61 32 32 35
Email bournet.b@chu-toulouse.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Description:

Pancreatic cancer represents the fourth cause of death by cancer in Western countries. In over 90% of cases, it is due to an adenocarcinoma. The only curative treatment for pancreatic cancer remains the surgical exeresis. This one can only be suggested as a curative treatment in only 10 to 15% of cases. Besides, prevention or screening is difficult to set up due to the absence of clearly identified risk factors or groups and to the absence of useful markers for the diagnosis in clinical practice. The research efforts in this area must face a double challenge: saving time while improving the diagnosis period and strengthen the therapeutic equipment. It is important to identify and characterise the new molecular markers applicable for a better diagnosis and/or treatment (especially the response factors to chemotherapy). The present project aims to enrich with fresh tumor tissue and somatic genetic analysis the existing propective collection BACAP in order to support support future research projects on: - the development of new diagnostic tools, - understanding the development of tumors of the pancreas - the development of new therapeutic targets - understanding the response to chemotherapy…


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date February 28, 2035
Est. primary completion date January 31, 2035
Accepts healthy volunteers
Gender All
Age group 18 Years to 120 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
France Béthune hospital center Béthune
France Haut-Lévêque Hospital Bordeaux
France Huriez Hospital Lille
France Jean Mermoz private hosptila Lyon
France Regional Cancer Center From Montpellier Montpellier
France Saint Eloi Hospital Montpellier
France PAU hospital Pau
France Rangueil hospital Toulouse

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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