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PRE- MISTIC: MRI and Cine Imaging to Improve Staging of Tumors in the Colon (PRE-MISTIC)

R

Radboud University Medical Center

Status

Not yet enrolling

Conditions

Colon Cancer

Treatments

Diagnostic Test: MRI and CT

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

At this moment, we use CT and endoscopy to clinically stage colon tumours. Unfortunately, the combination of these imaging techniques is highly inaccurate. 40% of advanced pathological colon tumours (so called T4 tumours) are not staged as a T4 tumour pre-operatively. Preoperative or neoadjuvant chemotherapy (NAC) has improved outcomes in other gastrointestinal cancers and seems to be a promising pretreatment for colon tumours. To implement NACin colon tumours, we first need to stage the colon tumours with much higher accuracy. MRI sequences and cine imaging hold promise to provide more accurate staging of colon tumours.

Enrollment

15 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with clinical suspicion for T3 or T4 tumor based on standard clinical work-up with endoscopy and CT-scan
  • Age > 18 years
  • WHO Performance status of 0-2

Exclusion criteria

  • Patients with contraindications for MRI
  • Patients with clinical contraindications to undergo colon surgery
  • Patients receiving neoadjuvant therapy prior to surgery
  • Patients with known allergy to iodine or gadolinium contrast
  • Patient with contra-indication for contrasts based on kidney failure Neoadjuvant therapy is currently not the standard of care for advanced colon carcinoma, and applied only in selected cases or as part of a clinical trial. Because neoadjuvant therapy could result in tumor regression, thus impacting the gold standard of histological examination, patients selected for neoadjuvant therapy are excluded from this study.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Imaging cohort
Experimental group
Description:
Patients participating in pilot study who will receive an additional MRI-scan, cineMRI and cineCT scan.
Treatment:
Diagnostic Test: MRI and CT

Trial contacts and locations

1

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Central trial contact

Richard ten Broek, MD, PhD

Data sourced from clinicaltrials.gov

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