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Microsphere Localization Using PET/MRI or PET/CT in Patients Following Radioembolization

Pilot Study of Microsphere Localization Using PET/MRI or PET/CT in Patients Following Radioembolization

Status
Terminated
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01744054
Enrollment
57
Registered
2012-12-06
Start date
2012-10-25
Completion date
2017-04-03
Last updated
2018-03-05

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

Conditions

Liver Neoplasms

Brief summary

The successful localization of the y90 microspheres by PET/MR and/or PET/CT scans would be a useful tool in individualizing patient care after the radioembolization procedure. The information from a PET/MR or PET/CT scan would allow for early evaluation of the technical success of the procedure.

Interventions

DEVICEPET/MR
DEVICEPET/CT

Sponsors

Washington University School of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participant must successfully complete the MRI screening form if receiving an MRI * Participant must be scheduled to undergo radioembolization for any indication * Participant must be ≥ 18 years of age * Participant must be able to understand and willing to sign an Institutional Review Board (IRB)-approved written informed consent document

Exclusion criteria

* Participant must not have any contraindications to MRI scanning * Patient must not be pregnant or breastfeeding * If agreeing to MRI contrast, participant must not have renal insufficiency (glomerular filtration rate (GFR \< 30 mL/min/1.73 m2) measured within the past 60 days * If agreeing to MRI contrast, participant must not be on dialysis * If agreeing to MRI contrast, participant must not have had a prior allergic reaction to gadolinium-based contrast agents * PET/MRI or PET/CT is not able to be scheduled within 72 hours of radioembolization

Design outcomes

Primary

MeasureTime frameDescription
Evaluate y90-PET/MRI and PET/CT for potential on reporting technical success of radioembolization1 day (one time event for patient)A diagnostic radiologist and a nuclear medicine physician will evaluate the images and will determine whether technical success of the procedure can be determined. They will rate the images if they are 'adequate' to report on these two measures.
Evaluate y90-PET/MRI and PET/CT for potential on reporting presence of extrahepatic deposition of microspheres1 day (one time event for patient)A diagnostic radiologist and a nuclear medicine physician will evaluate the images and will determine any presence of extrahepatic deposition of microspheres.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026