18F-Pentixafor PET in Hematologic Malignancies
Recruiting now
Conditions studied: Hematological Malignancies
In brief
The aim of this study is to evaluate the efficacy of 18F-Pentixafor PET imaging in the diagnosis, staging and response evaluation of hematological malignancies.
Key facts
- Study ID
- NCT07122674
- Run by
- First Affiliated Hospital of Zhejiang University
- People needed
- 100
- Starts
- 2025-07-01
- Expected to finish
- 2029-12-01
- Last updated by the study team
- 2025-08-14
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age of 18-80 years old, both sexes, with behavioral capacity;
- patients with suspected or confirmed hematological malignancies;
- 18F-FDG PET or other imaging examinations should be performed according to the treatment plan;
- For suspected patients, biopsy or needle biopsy is expected to obtain pathological results;
- Can provide informed consent, can understand and comply with the requirements of the study.
You may not qualify if…
- pregnant and lactating women;
- patients with fear or radiophobia, or with mental disorder or primary affective disorder;
- received ionizing radiation outside the scope of this study for clinical medical or scientific research purposes within the past year, resulting in an annual radiation exposure dose exceeding 50 mSv;
- received investigational drugs or devices of uncertain efficacy or safety within 1 month;
- Any condition that the chairpersons of the study consider that any link related to the study may cause harm or have potential harm.
Where it is running
- The First Affiliated Hospital of Zhejiang University School of Medicine — Hangzhou, Zhejiang, China (enrolling)
Full record on ClinicalTrials.gov
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