Using 68Ga-HA-DOTATATE PET/CT to Diagnose Neuroendocrine Tumors
Official title: 68Ga-HA-DOTATATE PET/CT in Adults With Neuroendocrine Tumors
Run by Alberta Health services · NCT05673031 · Data updated 2026-11-12
This study is testing a new type of imaging called 68Ga-HA-DOTATATE PET/CT to see if it can better diagnose certain neuroendocrine tumors compared to regular imaging methods.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 100 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Alberta Health services Academic / other |
| Locations | 1 site (Calgary, Alberta) |
| Status | Recruiting |
| Started | February 1, 2023 |
| Main results expected | January 1, 2027 |
| Study ends | January 1, 2027 |
| Registry record updated | January 5, 2023 |
| Trial ID | NCT05673031 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults aged 18 and older with clinically suspected or biopsy-proven neuroendocrine tumors.
✕Probably not a fit
Patients who are pregnant, nursing, or have had surgery in the area of interest within the last two months 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 68Ga-HA-DOTATATE PET/CT imaging in diagnosing somatostatin positive neuroendocrine tumors compared to conventional imaging methods such as CT, MRI, and other PET scans. It aims to determine the utility of this imaging technique in the primary workup of suspected neuroendocrine tumors and in the surveillance of completely resected tumors. Additionally, the study will assess its role in localizing functioning neuroendocrine tumors like insulinoma and gastrinoma. Participants will undergo imaging to compare results with standard diagnostic approaches.
Why it matters
Potential benefit: If successful, this imaging technique could improve the accuracy of diagnosing neuroendocrine tumors, leading to better patient management.
How similar studies have gone: While this approach is being evaluated, similar imaging techniques have shown promise in diagnosing neuroendocrine tumors, suggesting potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Male or female. If female of child-bearing potential and outside of the window of 10 days since the last menstrual period, a negative pregnancy test will be required. 2. Age greater than or equal to 18 years. 3. Able and willing to follow instructions and comply with the protocol. 4. Provide written informed consent prior to participation in the study. 5. Clinically suspected (patients presenting with symptom(s) suggestive of carcinoid syndrome or biochemically suggestive of Neuroendocrine Tumor) or Biopsy proven Neuroendocrine Tumor Exclusion Criteria: 1. Nursing or pregnant females. 2. Age less than 18 years. 3. Surgery in the area of interest within the preceding 2 months.
Where it's running
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Foothills Medical Center 1403 29 St NW
Calgary, Alberta, Canada Recruiting
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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.