Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
ID05428358

Incremental Value of Magnetic Resonance Imaging in Selection of Pancreatic Cancer Patients for Surgery (MAGIPAC)

Led by University of Aarhus · Updated on 2026-04-29

200

Participants Needed

3

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Aarhus

Lead Sponsor

R

Rigshospitalet, Denmark

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the added benefit of using magnetic resonance imaging (MRI) alongside computed tomography (CT) in diagnosing pancreatic cancer. This nationwide, prospective clinical trial aims to determine if MRI can better identify liver metastases in patients with pancreatic cancer to improve selection for surgery. The study is sponsored by the University of Aarhus and focuses on patients with locally resectable or borderline resectable tumors without liver metastases on CT. Participants will receive a preoperative MRI after their outpatient visit at the surgical clinic and before the scheduled surgery date. This diagnostic test is being evaluated to see if it changes treatment decisions compared to using CT alone. The study monitors patients through various timepoints including 1 week for treatment strategy changes and up to 3 years for survival and recurrence outcomes. During the study, participants undergo the MRI scan and are followed by researchers who assess treatment plans, surgical outcomes, survival rates, and healthcare costs. Key measurements include detection of liver metastases, surgery and resection rates within 1 month, and overall survival at 1 and 3 years. The total follow-up period extends to 3 years to track recurrence-free survival and long-term effects.

CONDITIONS

Brief Title

Incremental Value of Magnetic Resonance Imaging in Selection of Pancreatic Cancer Patients for Surgery

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pancreatic cancer patients considered to have a locally resectable or borderline resectable tumor by the local hepato-pancreato-biliary multidisciplinary team board
  • No liver metastases on CT scan
  • At least 18 years old and able to provide informed consent
  • Expected pancreatic ductal adenocarcinoma based on CT scan
Not Eligible

You will not qualify if you...

  • Presence of metastatic disease
  • Prior receipt of neoadjuvant chemotherapy or downstaging or downsizing treatment
  • Comorbidity that makes major surgery impossible (inoperable)
  • Lack of informed consent
  • Unable to undergo MRI due to kidney insufficiency (eGFR < 60 ml/min/1.73 m2), claustrophobia, or cardiac pacemaker
  • Postoperative histology not showing adenocarcinoma of pancreato-biliary origin
  • MRI with liver-specific contrast already performed during standard workup

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 1 week

Participants undergo magnetic resonance imaging (MRI) in addition to computed tomography (CT) to detect liver metastases before surgery.

1 visit (in-person)

Surgery

Duration - Up to 1 month

Participants undergo surgical resection based on imaging results and clinical assessment.

1 to 2 visits depending on surgical schedule

Long-term Monitoring

Duration - Up to 3 years

Participants are followed to assess overall survival, recurrence-free survival, and healthcare outcomes after surgery.

Periodic follow-up visits

Trial Site Locations

Total: 3 locations

1

Aalborg University Hospital

Aalborg, Denmark

Actively Recruiting

2

Aarhus University Hospital

Aarhus, Denmark, 8200

Actively Recruiting

3

Rigshospitalet

Copenhagen, Denmark

Actively Recruiting

Loading map...

Research Team

J

Jakob Kirkegård, MD, PhD

F

Frank Mortensen, MD, DMSc

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

Similar Trials

Evaluation of Diagnostic Value of 18F-T2 PET/ CT Imaging for...

Clear Cell Renal Cell Cancer (ccRCC)

Actively Recruiting

1 location

A Phase 1/2a Study Utilizing 64Cu-LNTH-1363S (64Cu Radiolabe...

Metastatic Sarcoma

Actively Recruiting

5 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here