18F-DOPA
OtherInjection of 18F-DOPA and PET / CT-scan assessment
NCT Number: NCT02856347
The aim of the trial is to study a radiating diagnosis agent used in post surgery when the biological assessment highlighted a residual disease.
This is an inter-regional multicentric, prospective study evaluating the benefit of PET F-DOPA imaging in involved node detection compared to standard imaging assessment in patient with medullary thyroid cancer.
The purpose of the study is to evaluate the impact and performance of a new PET / CT (computerized tomography ) tracer targeting dopamine receptor in patient with residual ganglionar biological disease after initial surgery of medullary thyroid cancer compared to standard imaging.
Obtained data will be compared to the "gold standard" based on :
* nodes cytology when they could be punctured * histology when a new surgery will be recommended * surveillance when the 2 first cases will be not applicable (imaging monitoring, evolution of thyrocalcitonin)
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
CHU Haut-Lévêque, Bordeaux, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Injection of 18F-DOPA and PET / CT-scan assessment
Time frame: up to 3 years
Analysis will be performed by node.
Time frame: up to 3 years
Analysis will be performed by patient.
Time frame: up to 3 years
Analyses will be performed by patient and by node.
Time frame: up to 3 years
Analyses will be performed by patient and by metastasis.
Time frame: up to 3 years
Comparison of the modification of care (orientation to a surgery or a surveillance) decided after standard imaging assessment following result of TEP-FDOPA exam.
Time frame: up to 3 years
Concordance (centre / reviewer) of PET F-DOPA result interpretation will be evaluated.
Institut Claudius Regaud
Other
Prospective Study Evaluating the Medullary Thyroid Cancer Management's Care Using PET ( Positron Emission Tomography) F-DOPA in Patients With a High Level of Postoperative Residual Thyrocalcitonin
Acronym: CMTpostopFDOPA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT01298323
Adenocarcinoma, Carcinoma
St Leonards, New South Wales, Australia
View Trial DetailsNCT05534594
Adenocarcinoma, Carcinoma
Groningen, Provincie Groningen, Netherlands
View Trial DetailsNCT03037385
Adenocarcinoma, Adenocarcinoma, Papillary
Phoenix, Arizona, United States
View Trial DetailsNCT06292988
Adenocarcinoma, Carcinoma
Oregon City, Oregon, United States
View Trial Details