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PAncreatic Disease Cohort of TOuLouse

PAncreatic Disease Cohort of TOuLouse

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05824403
Acronym
PACTOL
Enrollment
300
Registered
2023-04-21
Start date
2023-11-28
Completion date
2027-12-31
Last updated
2023-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Diseases

Keywords

Pancreatic cyst, Acute pancreatitis, chronic pancreatitis, Intra Pancreatic Mucinous Neoplasia, diagnosis

Brief summary

This study is a prospective cohort dedicated to pancreatic diseases excluding cancer. The aim is to develop positive or differential diagnostic tools between benign potentially malignant or malignant pancreatic pathologies. During this study the investigators collect data and biological samples to support research project.

Detailed description

This collection focuses on pathology of the pancreas requiring specific investigations or management for diagnosis or treatment. Pancreatic pathologies can be classified as malignant, potentially malignant or benign tumors. These can be solid or cystic. There is an inflammatory attack on the pancreas, generating acute pancreatitis in the acute period, if the inflammatory manifestations persist, chronic pancreatitis will develop. Some lesions may be at risk of malignancy during their evolution, it is therefore necessary to improve the performance of monitoring and diagnostic tools in order to adapt the management of patients.

Interventions

None listed

Sponsors

University Hospital, Toulouse
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Patients with inflammatory or cystic exocrine pancreatic pathology * Patient able to read and understand the information leaflet * Patients who have agreed to participate in the study and have signed the free and informed consent * Patients affiliated to a social security system (including AME)

Exclusion criteria

* Patient with pancreatic cancer pathology * Patients with active cancer, whatever the origin * Pregnant or breastfeeding patients * Patients under legal protection, guardianship or trusteeship

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic tools3 years after the first inclusionTo develop positive or differential diagnostic tools between benign potentially malignant or malignant pancreatic pathologies

Secondary

MeasureTime frameDescription
New targets3 years after the first inclusionTo identify new screening targets
Improvement of management3 years after the first inclusionTo improve the management of cystic lesions or Chronic pancreatitis on the decision of therapeutic management
Microbiota3 years after the first inclusionStudy of the microbiota of pancreatic diseases
Clinical data access3 years after the first inclusionTo make available to the scientific community quality material with associated clinical data also of quality

Countries

France

Contacts

Primary ContactBarbara BOURNET, MD
bournet.b@chu-toulouse.fr0561323235
Backup ContactCindy CANIVET
canivet.c@chu-toulouse.fr05 61 32 20 48

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026