99mTc-1-thio-D-glucose SPECT/CT Versus 18F-Fluoroethyl-l-tyrosine PET/CT in Brain Tumor Imaging (NCT07475390) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
99mTc-1-thio-D-glucose SPECT/CT Versus 18F-Fluoroethyl-l-tyrosine PET/CT in Brain Tumor Imaging
Russia40 participantsStarted 2026-02-15
Plain-language summary
An open-label, single-center study with 99mTc-1-thio-D-glucose single photon emission computed tomography / computed tomography (SPECT/CT) and 18F-fluoroethyl-l-tyrosine (18F-FET) positron emission tomography / computed tomography (PET/CT) in primary and recurrent glioma patients, where the primary endpoint of the study is to compare imaging properties of 99mTc-1-thio-D-glucose SPECT/CT and 18F-FET PET/CT of brain tumor Imaging.
Who can participate
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Diagnosis of primary and recurrent glioma;
* Sequential injection of 99mTc-1-thio-D-glucose and 18F-FET in the interval of 14 days in each patient;
* Hematological, liver and renal function test results within the following limits:
* White blood cell count: \> 2.0 x 109/L
* Hemoglobin: \> 80 g/L
* Platelets: \> 50.0 x 109/L
* Alanine aminotransferase (ALT), alkaline phosphatase (ALP), aspartate aminotransferase (AST): =\< 5.0 times Upper Limit of Normal
* Bilirubin =\< 2.0 times Upper Limit of Normal
* Serum creatinine: Within Normal Limits
* A negative pregnancy test for all patients of childbearing potential. Sexually active women of childbearing potential participating in the study must use a medically acceptable form of contraception for at least 30 days after study termination;
* Subject is capable to undergo the diagnostic investigations to be performed in the study;
* Informed consent.
Exclusion Criteria:
* Second, non-brain malignancy;
* Active current autoimmune disease or history of autoimmune disease;
* Active infection or history of severe infection within the previous 3 months (if clinically relevant at screening);
* Known HIV positive or chronically active hepatitis B or C;
* Administration of other investigational medicinal product within 30 days of screening;
* Ongoing toxicity \> grade 2 from previous standard or investigational therapies, according to US National Cancer Institute's.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
99mTc-1-thio-D-glucose uptake in tumor (SUVmean)
Timeframe: 1 hour
2
99mTc-1-thio-D-glucose uptake in background (SUVmean)
Timeframe: 1 hour
3
99mTc-1-thio-D-glucose tumor-to-background ratio (SPECT/CT)
Timeframe: 1 hour
4
Sensitivity of 99mTc-1-thio-D-glucose SPECT/CT (%)
Timeframe: 1 hour
5
18F-FET uptake in tumor (SUVmean)
Timeframe: 20 minutes
6
18F-FET uptake in background (SUVmean)
Timeframe: 20 minutes
7
18F-FET tumor-to-background ratio (PET/CT)
Timeframe: 20 minutes
8
Sensitivity of 18F-FET PET/CT (%)
Trial details
NCT IDNCT07475390
SponsorTomsk National Research Medical Center of the Russian Academy of Sciences