NCT06945432

Brief 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

Trial Health

87
On Track

Trial Health Score

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

Enrollment
27

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

July 1, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2025

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 5, 2025

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

April 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 25, 2025

Completed
Last Updated

April 25, 2025

Status Verified

February 1, 2025

Enrollment Period

9 months

First QC Date

April 18, 2025

Last Update Submit

April 18, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Lesion uptake

    Standardized uptake value (SUV)

    1 day

Eligibility Criteria

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

Malignant tumor patients diagnosed by histopathology and imaging

You may qualify if:

  • (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.

You may not qualify if:

  • (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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The Second Hospital of Lanzhou University

Lanzhou, Gansu, 730030, China

Location

MeSH Terms

Conditions

Neoplasms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr.

Study Record Dates

First Submitted

April 18, 2025

First Posted

April 25, 2025

Study Start

July 1, 2024

Primary Completion

March 31, 2025

Study Completion

April 5, 2025

Last Updated

April 25, 2025

Record last verified: 2025-02

Locations