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NCT07781306Recruiting

PrOspEctive Metastases Imaging (POEM)

Prospective Complete Histopathological Characterization of Liver Metastases From Colorectal and Breast Carcinoma to Predict the Histopathological Growth Patterns by Medical Imaging - PrOspEctive Metastases Imaging (POEM)

Source: ClinicalTrials.gov · Last updated 24 Aug 2026

Brief summary (registry, in English)

This is a non-interventional, observational study with an optional interventional biobanking activity. Liver metastases of patients undergoing partial hepatectomy will be sampled completely while respecting the orientation used for medical imaging, in order to correlate the histopathological growth patterns in a 3D-map with the imaging characteristics. The full pathological sampling will only use remnant tissue.

Status (registry)
Recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
15 Feb 2021
Start date
8 Sept 2020
Primary completion date
31 Dec 2027
Lead sponsor
Cancer Research Antwerp
NCT number
NCT07781306

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 8 Sept 2020 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients without MRI or CT of the liver prior to surgery
  • Prior radiofrequency ablation (RFA) or transarterial chemoembolization (TACE) on the liver metastasis that would be operated

Other

  • Time interval between medical imaging, CT and/or MRI is more than 12 weeks (nb: time interval is preferably less than 4 weeks but this is not an exclusion criterium)

Who the study is looking for

  • ≥ 18 years old.
  • Patients with liver metastatic colorectal or breast carcinoma undergoing a surgical excision of the liver metastases
  • Therapy-naive patients as well as patients with neo-adjuvant therapy are eligible for inclusion
  • Willingness of the patient to participate in this study demonstrated by signed written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
GZA St Augustinus
Coordinator of this site? Confirm its status
WilrijkBelgiumRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.