NCT06083103

Contribution of PET/MRI in Locally Advanced Cervical Cancer (ATICC)

Contribution of PET/MRI in Locally Advanced Cervical Cancer
Institut de cancérologie Strasbourg Europe·ClinicalTrials.gov·diagnostic testNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Cervical Cancer
Drug/Device/Intervention
18-FDG PET-MRI
Study type
Observational
Intervention type
diagnostic test
Sponsor & location
Primary sponsor
Institut de cancérologie Strasbourg Europe
Location
Strasbourg, France
Timeline & enrollment
Phase
N/A
Start date
Oct 02, 2023
End date
Dec 31, 2025
Enrollment
50 participants
Primary outcome

Compare performances of PET/MRI and PET/CT in the detection of lumbar aortic lymph node metastases in cervical cancer patients with tumors graded IB2 to IVA stage

Summary

[18 F]fluorodeoxyglucose (18F-FDG) positron emission tomography-magnetic resonance imaging
 (PET/MRI) is a new hybrid imaging tool that has recently arrived in oncology, and is
 particularly promising. Its usefulness seems obvious in certain tumor types, but its place in
 the staging of cervical cancers has never been explored in a prospective trial to our
 knowledge.
 
 Previously, a comparative retrospective study from 2009 found a better sensitivity of PET
 fused to diagnostic MRI images compared to PET/CT (positron emission tomography/computed
 tomography) in the detection of metastatic lymph nodes (54 and 44% respectively). It was an a
 posteriori fusion of images, from images acquired by PET-CT.

ICD-10 classifications
Severe cervical dysplasia, not elsewhere classifiedMild cervical dysplasiaModerate cervical dysplasiaCarcinoma in situ: Cervix, unspecifiedCervical root disorders, not elsewhere classified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06083103
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06083103 through Pure Global AI's free database. This phase not specified trial is sponsored by Institut de cancérologie Strasbourg Europe and is currently Not yet recruiting. The study focuses on Cervical Cancer. Target enrollment is 50 participants.

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