Actively Recruiting
Evaluation of 68Ga-DOTATOC PET/CT-enterography for the Detection of the Primary Lesion in Neuroendocrine Tumors of the Small Bowel
Led by European Institute of Oncology · Updated on 2025-01-14
18
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Neuroendocrine tumors of the small intestine (Si-NENs) are relatively rare cancers. Surgical removal is currently the only curative option for early-stage disease, but its role in advanced metastatic gastroenteropancreatic neuroendocrine tumors (GEP-NETs) is still debated. Accurate staging and assessment of tumor burden are critical for determining the correct disease stage and guiding appropriate treatment. A key feature of these tumors is the presence of somatostatin receptors, which can be targeted with special radiolabeled peptides for imaging purposes. This study evaluates the use of a specific imaging technique called 68Ga-DOTATOC PET/CT-enterography to detect primary lesions and multifocal tumors in the small bowel neuroendocrine tumors. Participants undergo this imaging procedure, which uses a radioactive tracer that binds to somatostatin receptors, providing detailed pictures that may be more precise than conventional imaging methods. The study aims to measure how sensitive and specific this imaging test is in identifying these tumors. During the study, participants will have the PET/CT-enterography scan with 68Ga-DOTATOC, and researchers will compare its results to other imaging methods to assess its accuracy. The main outcome is the ability of this imaging to detect the tumors within three months. This helps doctors understand how well this technique works for diagnosing small bowel neuroendocrine tumors and planning treatment. The study is sponsored by the European Institute of Oncology and includes adults aged 18 and older eligible for surgery.
CONDITIONS
Brief Title
Use of 68Ga-DOTATOC PET/CT-enterography for Detection of the Primary Lesion in Neuroendocrine Tumors of the Small Bowel
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with small bowel neuroendocrine tumors
- Tumors of any grade (1 to 3) and any Ki 67 percentage
- Patients eligible for surgical resection
You will not qualify if you...
- Patients with synchronous other oncological disease
- Patients with inflammatory bowel disease
- Patients not eligible for surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 3 months
Participants undergo PET/CT-enterography with 68Ga-DOTATOC to detect the primary lesion in neuroendocrine tumors of the small bowel.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
European Institute of Oncology
Milan, Italy
Actively Recruiting
Research Team
L
Luigi Funicelli, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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