PET CT

7

Review clinical trials related to PET CT. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Performance of Amino Acid PET in Brain Metastases

Differentiating radiation necrosis from tumor progression in patients with brain metastases has a major therapeutic and prognostic implications

Participants needed: 80
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Central Hospital, Nancy, FranceUpdated: Jun 30, 2026
Eligibility criteria

Patients who received a PET amino acid for differentiating radiation necrosis fr...

Patients who refused the using of their data

Status: Not yet recruiting

PET-CT in Lymphoma Among the Eldery

This study investigates PET-CT imaging patterns and metabolic parameters in elderly patients (≥60 years) diagnosed with lymphoma, aiming to enhance diagnostic accuracy and prognosis using 18F-FDG PET/CT scans.

Participants needed: 63
Trial details
Age: 60+Biological sex: AllType: ObservationalSponsor: Assiut UniversityUpdated: Dec 2, 2025
Eligibility criteria

Not listed

Status: Recruiting

Synthetic PET From CT Improves Precision Diagnosis and Treatment of Lung Cancer: a Prospective, Observational, Multicenter Study

This study aims to synthesise PET data that preserves biological relevance and adds clinical value to the diagnosis and prognosis of lung cancer by establishing anatomical-to-metabolic mapping based on paired diagnostic CT and FDG-PET scans, thereby prospectively validating the clinical utility of the model.

Participants needed: 10,000
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: Shanghai Pulmonary Hospital, Shanghai, ChinaUpdated: Nov 24, 2025Locations: 5
Eligibility criteria

Patients with non-small cell lung cancer scheduled to undergo PET-CT and patholo... [+1]

History of other malignant tumours; [+3]

Status: Recruiting

[18F]F-FAPI PET/CT and Laparoscopy in Staging Advanced Gastric Cancer

The goal of this clinical trial is to learn if a new type of scan, FAPI-PET/CT, can help find metastases of gastric cancer. We want to know how well this scan works for this purpose and whether it is less burdensome for patients compared to the methods we currently use to find metastases. The main questions it aims to answer are: * In how many patients can FAPI-PET/CT find metastases, which leads to a change in their treatment plan as decided by their medical team, such as avoiding unnecessary surgeries and changing from treatment meant to cure the disease to treatment focused on comfort (palliative treatment)? * In how many patients does FAPI-PET/CT change the diagnostic process as decided by their medical team, like more biopsies or imaging, or changing the type (extent) of surgery needed? Apart from the usual care gastric cancer patients receive, participants will: * Undergo one additional scan, which will take approximately 2 hours in total (excluding travel time) * Complete a number of questionnaires, which will take approximately 4 hours in total

Participants needed: 250
Trial details
Phase: Phase 2, Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Leiden University Medical CenterUpdated: Aug 27, 2025Locations: 10
Eligibility criteria

Histologically proven adenocarcinoma of the stomach or the esophagogastric junct... [+4]

Siewert type I-II esophagogastric junction tumor; [+7]

Status: Recruiting

68Ga-C1 PET/ CT Imaging in Clear Cell Renal Cell Carcinoma

The goal of this clinical trial is to evaluate the diagnostic value of CAIX protein specific probe 68Ga-C1 in PET/CT imaging in clear cell renal cell carcinoma patients. It will also learn about the safety, tolerability and radiation dosimetry of 68Ga-C1. Researchers will compare the diagnostic value of 68Ga-C1 PET/CT and 18F-FDG PET/CT in Chinese patients with indeterminate renal masses or confirmed clear cell renal cell carcinoma.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Peking University First HospitalUpdated: Nov 7, 2024Locations: 1
Eligibility criteria

Signed written informed consent; [+3]

Renal mass is known to be a metastasis of another primary tumor; [+6]

Status: Recruiting

Image Assisted Optimization of Proton Radiation Therapy in Chordomas and Chondrosarcomas

Rationale: Chordomas and chondrosarcomas located in the axial skeleton are malignant neoplasms of bone. These tumors share the same clinical challenges, as the effect of the disease is more a function of their local aggressiveness than their tendency to metastasize (20% metastasize). The local aggressive behavior can cause debilitating morbidity and mortality by destruction of nearby located critical neurovascular structures. Imaging has, in addition to histopathology, a role in diagnosis and in guiding (neo)adjuvant and definitive treatment. Despite the low sensitivity to radiotherapy, proton radiotherapy has been successfully used as an adjunct to resection or as definitive treatment for aggressive chordomas and chondrosarcomas, making it a standard indication for proton therapy in the Netherlands. Chordomas and chondrosarcomas consist, especially after previous therapy, of non-viable and viable tumor components. Identification of these viable components by functional imaging is important to determine the effect of previous therapy, as change in total tumor volume occurs more than 200 days after change of functional imaging parameters. Objective: The main objective of this study is to determine if functional MRI parameters change within 6 months, and earlier than volumetric changes after start of proton beam therapy. This would allow timely differentiation between affected and unaffected (viable) tumor components, which can be used for therapy adjustment. Secondary objectives: Determine which set of parameters (PET-CT and secondary MRI) can predict clinical outcome (tumor specific mortality, development of metastases, morbidity secondary to tumor activity and morbidity secondary to treatment); determine what type of imaging can accurately identify viable tumor nodules relative to critical anatomical structures; improving understanding of relevance of changing imaging parameters by correlating these with resected tumor. Study design: Prospective cohort study Study population: LUMC patients diagnosed with primary or recurrent chordoma or chondrosarcoma in the axial skeleton. A number of 20 new patients per year is expected. Main study parameters: Volumetric and functional MR imaging parameters including permeability parameters. Secondary parameters are generated by PET-CT (SUV, MTV and TLG), MR (perfusion, permeability and diffusion), therapy (proton beam dose mapping, surgery) and clinical outcome. End points are disease specific survival, progression free survival (including development of metastases), side effects of treatment, and functional outcome (see CRF). In patients who are treated with surgical resection following neo-adjuvant therapy, the surgical specimen will be correlated with imaging findings. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Treatment and clinical management will not be affected in this study, thus the additional burden, risks, and benefits associated with participation in this study are minimal. Two extra MRI and one PET-CT examination will be planned during proton therapy.

Participants needed: 40
Trial details
Age: 50+Biological sex: AllType: ObservationalSponsor: Leiden University Medical CenterUpdated: Nov 18, 2023Locations: 2
Eligibility criteria

Histologically diagnosed with primary or recurrent chordoma or chondrosarcoma in... [+1]

Diagnosis other than chordoma or chondrosarcoma is made. [+8]

Status: Recruiting

Fluciclovine PET/CT in Multiple Myeloma Patients

Comparison between image findings at aminoacid PET/CT and FDG PET/CT for myeloma patients

Participants needed: 10
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Oslo University HospitalUpdated: May 30, 2019Locations: 1
Eligibility criteria

Multiple myeloma patients suitable for ASCT treatment

Patients with contraindications to ASCT treatment