Using PET/CT imaging to diagnose GLP-1 receptor related diseases
Official title: Glucagon-like Peptide-1 Receptor PET/CT in GLP-1R Related Disease
Run by Tianjin Medical University · NCT06725693 · Data updated 2026-11-12
This study is testing a special imaging scan to see if it can help doctors better diagnose cancer in adults who may have diseases related to GLP-1 receptors.
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 | February 1, 2019 |
| Main results expected | November 1, 2027 |
| Study ends | November 1, 2027 |
| Registry record updated | September 8, 2026 |
| Trial ID | NCT06725693 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older with suspected or diagnosed malignant tumors related to GLP-1 receptor activity.
✕Probably not a fit
Patients with non-malignant lesions or those unable to provide informed consent will 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 observational study evaluates the effectiveness of 68Ga/18F-Exendin 4 positron emission tomography/computed tomography (PET/CT) in diagnosing primary and metastatic lesions in patients with GLP-1 receptor-related diseases. Participants include adults with suspected or newly diagnosed malignant tumors who are scheduled for an Exendin 4 PET/CT scan. The study measures the uptake of lesions using the maximum standard uptake value (SUVmax) and calculates various diagnostic metrics such as sensitivity and specificity.
Why it matters
Potential benefit: If successful, this study could enhance the accuracy of diagnosing GLP-1 receptor-related tumors, leading to better patient management.
How similar studies have gone: While this approach is innovative, similar studies using PET/CT imaging for tumor diagnosis have shown promising results.
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 Exendin 4 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: Qiusong Chen, MD
- Email: qs_c8@hotmail.com
- Phone: +862260362190
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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.