Clinical Trials Directory

Trials / Completed

CompletedNCT04306484

18F-DOPA-PET in Non-tumoral and Tumoral Brain Lesions

Status
Completed
Phase
Study type
Observational
Enrollment
74 (actual)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Background: 3,4-dihydroxy-6-\[18F\]-fluoro-L-phenylalanine (FDOPA) positron emission tomography (PET) can identify well low and high grade brain tumors. However, increased FDOPA uptake has been reported in non-tumoral brain lesions. The aim was to analyse FDOPA-PET in patients with non-tumoral brain lesions and to compare them with patients with (low and high grade) brain tumors. Methods: retrospective analyse. Patients consecutively recruited with suspected primary brain tumor (based on clinical and MRI findings) referred for FDOPA-PET at Nimes university Hospital between June 2015 and June 2019. FDOPA-PET parameters (maximum and mean lesion standardized uptake values \[SUV\] and ratios comparing lesion with different background uptake SUV) and thresholds were analysed in search for those offering optimal discrimination between non-tumoral and tumoral lesions.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTFDOPA-TEPFDOPA-TEP performed as part of the normal management of a suspected brain tumour

Timeline

Start date
2020-01-01
Primary completion
2020-12-31
Completion
2020-12-31
First posted
2020-03-13
Last updated
2025-12-04

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04306484. Inclusion in this directory is not an endorsement.