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Human Cerenkov Luminescence Imaging of Superficial In-Vivo Tumours after Administration of 18F-FDG

Human Cerenkov Luminescence Imaging of Superficial In-Vivo Tumours after Administration of 18F-FDG - Feasibility of In-vivo Human Cerenkov Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42215
Enrollment
12
Registered
2015-04-13
Start date
2015-04-22
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Cancer malignant tumours

Interventions

None listed

Sponsors

Nederlands Kanker Instituut
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients, older than 18 years, who will receive and 18F-FDG PET-CT scan and have a superficial tumour,

Exclusion criteria

Exclusion criteria: Patient younger than 18 years. Patients with a melanoma with a high melanin level.

Design outcomes

Primary

MeasureTime frame
The main question is whether we ara able to image the uptake of 18F-FDG in a human tumour, in-vivo, with a stand alone EMCCD camera. The primary study parameter is if we can subjectively distinguish the tumour from the background.

Secondary

MeasureTime frame
Secondary study parameters are the signal to noise ratio between the tumour and healthy tissue. With that we take the actual uptake and the depth of the tumour into account.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)