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Pilot study: The use of PET-MRI in the follow-up of RFA treated colorectal liver metastases

Pilot study: The use of PET-MRI in the follow-up of RFA treated colorectal liver metastases - PET-MRI after RFA

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON38868
Enrollment
20
Registered
2013-06-07
Start date
2013-07-15
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Local site recurrence after radiofrequency ablation of colorectal liver metastases

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Histological or cytological documentation of primary colorectal tumor Radiological or histological prove of one or more CRLM or radiological prove of a LSR after previous RFA/MWA treatment for CRLM CRLM or LSR treated with RFA/MWA or RFA/MWA in combination with resection Follow-up imaging performed in VUmc medical centre Age ³ 18 years Life expectancy of at least 1 year eGFR > 60 or hydration according to protocol before scanning

Exclusion criteria

Exclusion criteria: Cirrosis or steatosis Chemotherapy * 6 weeks before scanning (during the entire study) Pregnant or breast-feeding subjects Allergy to contrast media Patients developing recurrent intrahepatic disease that require resection of the ablated lesion eGFR

Design outcomes

Primary

MeasureTime frame
Primary outcome is the ability of PET-MRI in the detection of LSR in the liver compared to ceCT of the liver and PET-CT referred to histological findings or clinical follow-up.

Secondary

MeasureTime frame
Secondary outcomes are the inter-observer variability, the ability to diagnose new intrahepatic lesions and in what way PET-MRI is able to influence future treatment compared to PET-CT and ceCT. The patients satisfaction concerning the PET-MRI will be examined with a questionnaire.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)