Introduction of Y90-PET-CT Post Radioembolisation Therapy Scans
Recruiting
N/AInterventional Study
Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
10 (estimated)
Sponsor
The Christie NHS Foundation Trust · Other
Who this trial is looking for
This trial is looking for patients who are receiving Y90-microspheres therapy for liver tumors. Participants will undergo a special scan after their treatment to help doctors see how well the therapy is working.
Are You a Good Fit for This Trial?
You may be able to join if
I am undergoing Y90-microspheres therapy for liver treatment.
I am between 18 and 85 years old.
You may not be able to join if
I have a history of claustrophobia.
I cannot lie flat and still on my back for up to 45 minutes.
The clinical team thinks I might not follow the study rules.
I am pregnant or could become pregnant.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Yttrium-90, attached to microspheres, usually referred to as 90Y-microspheres or Y-90 radioembolisation, can be used in some cases to treat patients with liver tumours or liver metastasis. The treatment aim is to infuse the 90Ymicrospheres into the patient's liver. The microspheres get trapped in the lesions of micro-blood vessels while the yttrium-90, a radioactive compound, delivers radiation do…
Yttrium-90, attached to microspheres, usually referred to as 90Y-microspheres or Y-90 radioembolisation, can be used in some cases to treat patients with liver tumours or liver metastasis. The treatment aim is to infuse the 90Ymicrospheres into the patient's liver. The microspheres get trapped in the lesions of micro-blood vessels while the yttrium-90, a radioactive compound, delivers radiation doses locally at these sites and damages the diseased cells.
Therapy is performed in such a way the 90Y-microspheres are localised in the tumour areas minimising damage to the healthy liver tissue. This treatment requires many steps involving professionals from different medical disciplines.
Patients are scanned in the nuclear Medicine Department on a gamma camera the day after the treatment. This scan is referred as Y-90 bremsstrahlung-SPECT. This posttherapy scan provides a 3-dimensional (3D) image of the distribution of the therapeutic agent in the patient's abdomen so an assessment of how much of the therapeutic agent has gone to the sites of disease can be performed.
In this research project, the investigators would like to evaluate an alternative post-therapy scan to the one routinely performed on the gamma camera. The alternative scan is done on a PET-CT scanner and is referred to as Y90-PET-CT. This type of scan has been reported to provide improved quality images, providing more accurate information on the distribution of the patients therapeutic dose.
For this research project, the investigators will invite a small number of patients undergoing this therapy to be scanned twice after treatment: with the current post-therapy scan on a gamma camera; and with the newly proposed scan method, Y90-PET-CT. Depending on the outcomes of this project, assessed by an expert panel of radiologists and medical physicists, the investigators will determine whether we will introduce this new scanning method into clinical practice in the future.
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Eligibility Criteria
Inclusion Criteria:
* Patients undergoing liver treatment Y90-Microspheres therapy.
* Male or female
* Aged 18-85 years
Exclusion Criteria:
A participant will not be eligible for inclusion in this study if any of the following criteria apply:
* History of, or suffers from, claustrophobia or part…
Inclusion Criteria:
* Patients undergoing liver treatment Y90-Microspheres therapy.
* Male or female
* Aged 18-85 years
Exclusion Criteria:
A participant will not be eligible for inclusion in this study if any of the following criteria apply:
* History of, or suffers from, claustrophobia or participant feels unable to lie flat and still on their back for a period of up to 45 minutes in the scanner;
o Priority will be given to their current clinical care scan Y-90-bremsstrahlung-SPECT
* In the opinion of the clinical team, they are unlikely to comply with the study protocol and restrictions that it imposes (i.e. patient uncomfortable to withstand a double scan on the day); Female participants of childbearing potential must confirm they are not pregnant (a strict requisite before 90Y-therapy anyway).
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