Evaluating Tau PET/CT for Diagnosing Tau-Related Diseases
Official title: Tau PET/CT in Various Tau-Related Disease Patients
Run by Tianjin Medical University · NCT06690983 · Data updated 2026-11-12
This study is testing a new type of imaging scan to see if it can help doctors better diagnose Tau-related diseases in adults with suspected or diagnosed tumors.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Tianjin Medical University Academic / other |
| Locations | 3 sites (Hefei, Anhui and 2 other locations) |
| Status | Recruiting |
| Started | August 1, 2018 |
| Main results expected | November 1, 2027 |
| Study ends | December 1, 2027 |
| Registry record updated | September 8, 2026 |
| Trial ID | NCT06690983 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adult patients with suspected or newly diagnosed malignant tumors related to Tauopathies.
✕Probably not a fit
Patients with non-malignant lesions or those unable to provide informed consent may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of 18F-S16/T807 positron emission tomography/computed tomography (PET/CT) in diagnosing primary and metastatic lesions in patients with various Tau-related diseases. Participants, who are adults with suspected or diagnosed malignant tumors, undergo PET/CT scans to assess lesion uptake and quantify results using maximum standard uptake value (SUVmax). The study aims to calculate key diagnostic metrics such as sensitivity, specificity, and accuracy of the imaging technique.
Why it matters
Potential benefit: If successful, this study could enhance the diagnostic accuracy for patients with Tau-related diseases, leading to better treatment decisions.
How similar studies have gone: While this approach is novel in the context of Tau-related diseases, similar imaging techniques have shown promise in other neurodegenerative conditions.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: \- (i) adult patients (aged 18 years or order); (ii) patients with suspected or new diagnosed or previously treated malignant tumors (supporting evidence may include MRI, CT, tumor markers and pathology report); (iii) patients who had scheduled Tau PET/CT scan; (iv) patients who were able to provide informed consent (signed by participant, parent or legal representative) and assent according to the guidelines of the Clinical Research Ethics Committee. Exclusion Criteria: \- (i) patients with non-malignant lesions; (ii) patients with pregnancy; (iii) the inability or unwillingness of the research participant, parent or legal representative to provide written informed consent.
Where it's running
-
The First Affiliated Hospital of University of Science and Technology of China
Hefei, Anhui, China Recruiting -
The Affiliated Hospital of Qingdao University
Qingdao, Shandong, China Recruiting -
Tianjin Medical University General Hospital
Tianjin, Tianjin Municipality, China Recruiting
Study contacts
- Study coordinator: Ying Wang, MD
- Email: macrossplusvoices@163.com
- Phone: +8618702292537
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.