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Introduction of Y90-PET-CT Post Radioembolisation Therapy Scans

Sponsor: The Christie NHS Foundation Trust

NCT ID: NCT06123676

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Y90-PET-CT scan (device)
How long the study runs
Study runs about 31 months (dates as stated)
About the drug or intervention
Y90-PET-CT scan — device: 40 min extra PET-CT scan - no extra injection of radiotracer.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years to 80 Years
Who
All
Number of participants
10
Started
2023-10-09
Last checked
2024-11

Plain English Summary

What is this study?

  • • Testing a new treatment for cancer
  • • NA - 10 participants
  • • 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

Who can take part?

  • • Ages 18 Years to 80 Years
  • • Diagnosed with cancer

Where?

  • • Manchester - The Christie NHS - Nuclear Medicine Department

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

More detail

The study will be conducted on patients with liver cancer and/or liver metastasis, referred to as 90Y-microspheres radiation therapy or Y-90 radioembolisation. There will be 10 patients recruited. No further radioisotope administration will be performed (please refer to section 7 for full eligibility criteria). Primary Outcome - Introduce and optimise a Y90-PET-CT protocol post-therapy scan for patients undergoing 90Y-radioembolisation treatment. The Y90-PET-CT scan will be used primarily to confirm the radiotracer delivery to the target lesions. A Y90-PET-CT scan is believed to provide improved quality images compared to a Y90-bremsstrahlung-SPECT scan; hence, more accurate information on the success/failure of the therapy is expected to be obtained when using Y90-PET-CT images. Secondary Outcomes - Introduce in the department post-therapy dosimetry for Y90-microspheres radioembolisation using the optimised 90Y-PET-CT images obtained from the primary objective. This work will be done following published guidelines for post-therapy dosimetry and using pre-existing and bespoke commercial software applications that perform this task. The investigators expect the images resulting from 90Y-PET-CT will provide better information about the success or not of the infusion of the 90Y-microspheres into the target areas. 90Y-PET-CT will, in turn, provide a better understanding of post-therapy scans in our department, better management of 90Y-radioembolization patients and the development of improved radioembolization treatment-planning models in the future.

Cancer

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years - 80 Years
  • Who can join: All genders

What the study is looking for

  • ✓Patients undergoing liver treatment Y90-Microspheres therapy.
  • ✓Male or female
  • ✓Aged 18-85 years

Who cannot take part

  • ✗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...
  • ✗o Priority will be given to their current clinical care scan Y-90-bremsstrahlung-SPECT
See the full 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 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).

Where Is This Study? (1 UK site)

The Christie NHS - Nuclear Medicine Department

Manchester M204BX, United Kingdom

Recruiting
Site contact (verified)
Jose M Anton Rodriguez, PhD01619187118Jose.antonrodriguez@nhs.net

How to Get in Touch

Heather Williams

Sponsor contact

CONTACT

01619187118 heather.williams34@nhs.net
Data sourced from ClinicalTrials.gov · Last verified: 2024-11