Assessment of Hypoxia Before Radioembolization Treatment With 18F-FMISO PET
NCT ID: NCT06027021
Last Updated: 2024-07-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
64 participants
OBSERVATIONAL
2023-08-15
2024-07-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Treatment group
Patients received radioembolization with hepatocellular cancer or colorectal cancer liver metastases
18F-Fluoromisonidazole PET
Imaging of hypoxia before radioembolization with 18F-Fluoromisonidazole PET.
Interventions
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18F-Fluoromisonidazole PET
Imaging of hypoxia before radioembolization with 18F-Fluoromisonidazole PET.
Eligibility Criteria
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Inclusion Criteria
* Is not eligible for surgery
* Above 18 years old
* The patients who are referred for transarterial radioembolization treatment to Ankara University School of Medicine Department of Nuclear Medicine.
Exclusion Criteria
* Claustrophobia
* Life expectancy shorter than 3 months
* Pregnant or breast-feeding patients
18 Years
ALL
No
Sponsors
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Ankara University
OTHER
Responsible Party
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Cigdem Soydal
Asc Prof
Principal Investigators
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Cigdem Soydal, MD
Role: PRINCIPAL_INVESTIGATOR
Ankara University
Locations
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Ankara University
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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ARTE-MISO
Identifier Type: -
Identifier Source: org_study_id
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