NCT06055010

Brief Summary

The goal of the IMPACT project is to set up a data sharing infrastructure between expert centers for pancreatic surgery that enables training, testing and validation of computer science tools to improve quality of care for patients with pancreatic cancer.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
45mo left

Started Jan 2014

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

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 Progress77%
Jan 2014Dec 2029

Study Start

First participant enrolled

January 1, 2014

Completed
9.4 years until next milestone

First Submitted

Initial submission to the registry

May 30, 2023

Completed
4 months until next milestone

First Posted

Study publicly available on registry

September 26, 2023

Completed
6.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2029

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2029

Last Updated

September 26, 2023

Status Verified

September 1, 2023

Enrollment Period

16 years

First QC Date

May 30, 2023

Last Update Submit

September 22, 2023

Conditions

Keywords

Artificial IntelligenceData ScienceComputer SciencePancreatic Cancer

Outcome Measures

Primary Outcomes (1)

  • Subproject dependent

    Endpoints within this project are dependent on the specific subprojects. This study will facilitate the collection of large amounts of real-world data for (future) computer science projects.

    Through study completion, an average of 5 years.

Study Arms (2)

Healthy individuals

Healthy individuals who received an abdominal CT-scan (controls).

Other: No interventions

Individuals with pancreatic lesions

Patients who received diagnostic procedures and/or treatment for (suspected) benign and malignant pancreatic lesions as registered in the Dutch Pancreatic Cancer Project (PACAP) audit database

Other: No interventions

Interventions

Considering the retrospective nature of this project and use of existing clinical and technical data, this project contains no interventions or prospective inclusion of healthy subjects / patients for the execution of experiments.

Healthy individualsIndividuals with pancreatic lesions

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients who underwent diagnostic procedures and/or treatment for (suspected) benign and malignant pancreatic lesions as registered in the Dutch Pancreatic Cancer Project (PACAP) audit database, as well as healthy individuals who received an abdominal CT-scan (controls).

You may qualify if:

  • ≥18 years of age
  • Patients who received diagnostic procedures and/or treatment for (suspected) benign and malignant pancreatic lesions as registered in the Dutch Pancreatic Cancer Project (PACAP) audit database and healthy individuals who received an abdominal CT-scan (controls)

You may not qualify if:

  • \- Subjects who object to the use of their data for the purpose of scientific research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Regional Academic Cancer Center Utrecht

Utrecht, 3584 CX, Netherlands

RECRUITING

MeSH Terms

Conditions

Pancreatic NeoplasmsPancreatic CystPancreatic Diseases

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsEndocrine Gland NeoplasmsDigestive System DiseasesEndocrine System DiseasesCysts

Central Study Contacts

Lois A Daamen, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

May 30, 2023

First Posted

September 26, 2023

Study Start

January 1, 2014

Primary Completion (Estimated)

December 31, 2029

Study Completion (Estimated)

December 31, 2029

Last Updated

September 26, 2023

Record last verified: 2023-09

Locations