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CompletedNCT06945432Updated Apr 25, 2025

Comparing 68Ga-CTR-FAPI and 18F-FDG PET/ CT in Cancer Detection

An observational study in Tumors, PET / CT and FDG PET/CT, sponsored by Lanzhou University Second Hospital. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-04-25.

Sponsored by Lanzhou University Second Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
27
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to compare the diagnostic efficacy of 68Ga-CTR-FAPI PET/CT and 18F-FDG PET/CT in various malignant tumors

Read the detailed description

This study recruited malignant tumor patients diagnosed by histopathology and imaging at the Nuclear Medicine Department of Lanzhou University Second Hospital from July 2024 to March 2025. The enrolled patients underwent 68Ga-CTR-FAPI PET/CT and 18F-FDG PET/CT scans within one week.

02

Conditions studied

  • Tumors
  • PET / CT
  • FDG PET/CT
  • FAPI
03

In context

Lead sponsor

Lanzhou University Second Hospital is the lead sponsor of 12 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Malignant tumor patients diagnosed by histopathology and imaging

Inclusion criteria

(a) Age ≥ 18 years old; (b) Suspected or newly diagnosed malignant tumors, evaluating the therapeutic effect of the tumor, or discovering recurrence/metastasis; (c) Obtain approval from oncologists and agree to undergo 18F-FDG and 68Ga-CTR-FAPI PET/CT scans within one week.

Exclusion criteria

Exclusion Criteria:

(a) Pregnancy or lactation period; (b) Claustrophobia. (c) Serious health problems: such as severe heart, liver and kidney dysfunction, diseases that affect the metabolism or clearance of imaging agents.

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
27 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Lesion uptake

    Standardized uptake value (SUV)

    Time frame: 1 day

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Study locations

1 site
  • The Second Hospital of Lanzhou University
    Lanzhou, Gansu 730030, China
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06945432
Lead sponsor
Lanzhou University Second Hospital
Responsible party
Yuxi Zhang (Dr., Lanzhou University Second Hospital) — Principal investigator
First posted
Apr 25, 2025
Start date
Jul 1, 2024
Primary completion
Mar 31, 2025
Completion
Apr 5, 2025
Last update
Apr 25, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2025. You cannot join it, but the record below documents what was studied.

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