Loading clinical trials...
Loading clinical trials...
The hypothesis for this study is that there is a dose-response relationship in patients treated with 177Lu-DOTATATE for meningiomas.
Dosimetry is essential for Peptide Receptor Radionuclide Therapy (PRRT) of meningiomas, to predict efficacy and dose-effect relationships at the individual level, and to move towards personalized medicine. Due to the increasing therapeutic applications of Lutathera, the European Association of Nuclear Medicine (EANM) recently issued recommendations on the dosimetry of 177Lu-labeled somatostatin analogues. Nevertheless, despite these recommendations, the evaluation of meningioma tumor dosimetry in Peptide Receptor Radionuclide Therapy studies is not systematic, which has not enabled us to clearly determine the dose delivered to the meningioma lesion in these treatments and the possible dose-response relationship in this type of treatment.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
CHRU de NANCY
Vandœuvre-lès-Nancy, France
Nuclear medicine Department CHRU de NANCY
Vandœuvre-lès-Nancy, France
Start Date
November 1, 2024
Primary Completion Date
January 1, 2025
Completion Date
February 25, 2025
Last Updated
March 4, 2025
11
ACTUAL participants
tumoral dosimetry by scintigraphy
DIAGNOSTIC_TEST
Lead Sponsor
Central Hospital, Nancy, France
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions