NCT07602569

Brief Summary

Glutamine is a crucial nutrient for cancer cell growth, and its metabolism is frequently dysregulated in malignancies. 18F-FGln is a PET tracer that targets this altered glutamine metabolism. However, there are currently limited studies on the diagnostic value of 18F-FGln PET/CT in various types of cancer. Therefore, this prospective study was conducted to investigate the value of 18F-FGln PET/CT in patients with various types of malignant tumors.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for all trials

Timeline
31mo left

Started Oct 2025

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress19%
Oct 2025Dec 2028

Study Start

First participant enrolled

October 20, 2025

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

May 16, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 22, 2026

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2028

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2028

Last Updated

May 22, 2026

Status Verified

August 1, 2025

Enrollment Period

2.8 years

First QC Date

May 16, 2026

Last Update Submit

May 16, 2026

Conditions

Keywords

cancer

Outcome Measures

Primary Outcomes (2)

  • SUVMAX

    Xingxiang's Chinese report system automatically delineates the areas of interest.

    Within one day after the PET/CT scan

  • TBR

    Xingxiang's Chinese report system automatically delineates the areas of interest.

    Within one day after the PET/CT scan

Study Arms (1)

Patients with Malignant Tumors

Patients with suspected or histopathologically confirmed malignant tumors who underwent 18F-FGln PET/CT scan at the Affiliated Cancer Hospital \& Institute of Guangzhou Medical University

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

This study will include patients from the Affiliated Cancer Hospital \& Institute of Guangzhou Medical University who underwent an 18F-FGln PET/CT scan between October 2025 and January 2028 . Eligible participants are adult patients aged 18 to 70 years with suspected or histopathologically confirmed malignant tumors. Patients with non-malignant lesions, pregnant women, and those with incomplete medical records or missing histopathological reference standards will be excluded. Data will be collected by reviewing the institutional medical records and PET/CT imaging database.

You may qualify if:

  • Patients undergoing tumor staging or evaluating treatment effect using 18F-FDG PET/CT or 18F-FGln PET/CT to determine the most appropriate treatment strategy
  • Patients without other tumor history
  • Patients with good compliance, providing informed consent, and able to follow the research protocol

You may not qualify if:

  • pregnant or lactating patients or patients under 18 years old
  • the subjects and their parents or legal representatives are unable or unwilling to provide written informed consent;
  • patients with poor compliance, unable to tolerate or cooperate with PET/CT examinations.
  • those who have undergone gastrointestinal barium meal examination within one week;
  • other situations where the investigators consider it inappropriate for the subjects to participate in this clinical trial

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Affiliated Cancer Hospital & Institute of Guangzhou Medical University

Guangzhou, China

RECRUITING

MeSH Terms

Conditions

Neoplasms

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
6 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head of Nuclear Medicine Department

Study Record Dates

First Submitted

May 16, 2026

First Posted

May 22, 2026

Study Start

October 20, 2025

Primary Completion (Estimated)

August 1, 2028

Study Completion (Estimated)

December 1, 2028

Last Updated

May 22, 2026

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations