Clinical trial Recruiting at 1 site Observational Ages 30 to 74

Delayed Ga-68 DOTATATE PET/MR for Detecting Liver Metastases in GEP-NETs

Official title: Incremental Value of Delayed 68Ga-DOTATATE PET/MR in the Detection of Liver Metastases From Gastroenteropancreatic Neuroendocrine Tumors

Run by First Affiliated Hospital of Fujian Medical University · NCT07898904 · Data updated 2026-11-12

This study tests whether a delayed Ga-68 DOTATATE PET/MR scan can better detect liver metastases in gastroenteropancreatic neuroendocrine tumors compared with the standard Ga-68 DOTATATE PET/CT.

Quick facts

Study typeObservational
Ages30 Years to 74 Years
SexAll
Enrollment46 (estimated)
SponsorFirst Affiliated Hospital of Fujian Medical University
Academic / other
Locations1 site (Fuzhou, Fujian)
StatusRecruiting
StartedDecember 1, 2023
Main results expectedDecember 31, 2026
Study endsApril 30, 2027
Registry record updatedOctober 27, 2026
Trial IDNCT07898904 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–80 with histologically confirmed well-differentiated GEP-NET and confirmed or suspected liver metastases, and with available comprehensive prior surgical, pathological, and follow-up data.

Probably not a fit

Patients without liver metastases or with lesions not better characterized by PET/MR may not experience a diagnostic benefit.

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 compares delayed Ga-68 DOTATATE PET/MR with conventional Ga-68 DOTATATE PET/CT for identifying liver metastases in adults with well-differentiated GEP-NETs. It aims to determine diagnostic performance in cases where liver lesions are small or of low avidity. Eligible participants have histologically confirmed GEP-NETs and suspected liver metastases, with comprehensive surgical, pathological, and follow-up data available. The analysis assesses whether PET/MR offers added value over PET/CT for staging and management decisions. The study is conducted at a single institution in Fujian, China and is led by the First Affiliated Hospital of Fujian Medical University.

Why it matters

Potential benefit: If successful, delayed Ga-68 DOTATATE PET/MR could improve detection of liver metastases and inform more accurate treatment planning for GEP-NET patients.

How similar studies have gone: Previous work supports Ga-68 DOTATATE PET/CT as a diagnostic standard, while the added value of delayed PET/MR remains to be clarified in this setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

(a)Histologically confirmed well-differentiated GEP-NETs via biopsy or surgical resection in adults aged 18-80 years,(b) confirmed or suspected liver metastases, as determined by previous imaging studies or PET/CT scans,(c) availability of comprehensive surgical reports, pathological findings, comparative data, and clinical follow-up outcomes for analysis,(d) absence of PET/MR contraindications , with voluntary participation and signed informed consent forms adhering to ethical and research guidelines

Exclusion Criteria:

(a) unavailability of surgical, pathological or long-term follow-up data; (b) non-compliance with age eligibility criteria or presence of comorbidities compromising protocol adherence

Where it's running

  • Department of Nuclear Medicine, the First Affiliated Hospital, Fujian Medical University
    Fuzhou, Fujian, China
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.