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Completed No phase listed Observational

[18F]FET PET for Characterization of Progressive or Recurrent Glioma From Treatment Related Changes

ClinicalTrials.gov ID: NCT07238322

Public ClinicalTrials.gov record NCT07238322. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 21, 2026, 12:34 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Assessment of the Efficacy of Floretyrosine F 18 ([18F]FET) Positron Emission Tomography (PET) for Characterization of Progressive or Recurrent Glioma From Treatment Related Changes

Study identification

NCT ID
NCT07238322
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Telix Pharmaceuticals (Innovations) Pty Limited
Industry
Enrollment
253 participants

Conditions and interventions

Interventions

  • 18F(FET)PET Diagnostic Test

Diagnostic Test

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 21, 2025
Primary completion
Jan 22, 2026
Completion
Jan 22, 2026
Last update posted
May 14, 2026

2025 – 2026

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
University of California, San Francisco San Francisco California 94107

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07238322, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 14, 2026 · Synced May 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07238322 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →