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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03980418
Other study ID # PSS2019/VERIDAT-VERGER-VS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 5, 2019
Est. completion date September 3, 2020

Study information

Verified date September 2020
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The semiconductor (cadmium-zinc-telluride, CZT) cameras significantly increase detection sensitivity in Single Photon Emission Computer Tomoscintigraphy (SPECT)(1) . The clinical routine applications of these cameras are today mainly limited to myocardial tomoscintigraphy with CZT dedicated cameras. Several studies whose one was done in Hospital of Nancy, made it possible to demonstrate a good diagnosis agreement between conventional cameras and semiconductor cameras in this indication, with better image quality obtained with semiconductor cameras (2). Today, so-called "wide field" semiconductor cameras are available in the clinic and allow for any type of SPECT examination. A comparative study between conventional and semiconductor cameras has been conducted for bone scintigraphy, and shows diagnostic superiority with this new type of camera (3). In addition, the new VERITON-CT ™ (Spectrum Dynamics Medical) camera has 12 mobile CZT-based detectors positioned around the patient allowing tomographic acquisitions and focusing the acquisition on the organ studied. This camera has a sensitivity of detection higher than that of conventional cameras and thus reduces the activity injected into the patient and / or the recording time. To date, no study has compared the two types of cameras in nuclear neurology and in particular, for the SPECT DaTSCAN ™ imaging of the pre-synaptic dopaminergic pathway. DaTSCAN ™ exam is used in clinical routine: 1. for the diagnosis of Parkinson's disease or related diseases when in doubt with an essential tremor (4) or 2. if suspicion of Lewy body disease, if in doubt with Alzheimer's disease (5). If the interpretation of DaTSCAN ™ exam is first visual, the quantification may increase accuracy diagnosis (6). Also, the database creation specific to each type of camera is recommended(7). The purpose of this study is to compare the diagnostically relevant informations and the quantitative analysis provided by the DaTSCAN™ SPECT, recorded on the conventional camera and recorded on the semiconductor camera VERITON-CT™


Description:

The clinical study is monocentric, interventional, non randomized, with minimal risk and constraints. All patients going to the nuclear medicine department for a DaTSCAN exam will be able to participate in this study if they understood study informations given by the physician and if they signed the inform consent. In first, patients will have a DaTSCAN™ SPECT on a conventional camera and after, they will have DaTSCAN™ SPECT on VERITON-CT™ camera with two records: one in focus striatum mode and the second in focus brain mode. The attenuation correction will be made with the computer tomography (CT) recorded at the same time as the SPECT (SPECT/CT)


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date September 3, 2020
Est. primary completion date September 3, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - all patients over 18 years sent to Datscan SPECT/CT - patients understanding and having signed the informed consent form. - without contraindication to have the scintigraphy - patient subject to a medical benefits scheme Exclusion Criteria: - known allergy to the one of the components of Datscan - pregnant, parturient or breastfeeding woman - major person under legal protection (any form of public guardianship) - major person unable to express consent - person deprived of liberty due to judicial or administrative decision.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
DaTSCAN SPECT/CT in VERITON-CT camera
the intervention is based on two recordings in camera VERITON-CT ; the first, in focus striatum mode and the second in brain focus mode

Locations

Country Name City State
France CHRU of Nancy Vandoeuvre les Nancy cedex

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other Degree of concordance (Kappa) of the exams results of different recordings comparison between the exam results (positive diagnosis of Parkinson disease versus differential diagnosis) in conventional camera and the one obtained with the VERITON-CT in striatum focus mode 16 months
Other Degree of concordance (Kappa) of the exams results of different recordings comparison between the exam results (positive diagnosis of Lewy bodies dementia versus differential diagnosis) in conventional camera and the one obtained with the VERITON-CT in striatum focus mode 16 months after the first enrollment
Other ratios of uptake obtained with conventional camera and on the striatum focus record with VERITON-CT the uptake ratios are:caudate nuclei/occipital cortex, putamen/occipital cortex, to the right and caudate nuclei/medium cingulate cortex, putamen/medium cingulate cortex to left, obtained with conventional camera and on the striatum focus record with VERITON-CT camera immediately after SPECT-CT exam
Other quality scores of images from conventional camera and from VERITON (striatum) 0= very bad quality and impossible to do a diagnosis, 1=bad quality and difficult diagnosis, 2= medium quality, 3 = good quality and 4= excellent quality immediately after SPECT-CT exam
Other recording activity in striatal area for the images from conventional camera and from VERITON (striatum) recorded activities will be reported by injected MBq for the images obtained with the conventional camera and with VERITON striatum focus record immediately after SPECT-CT exams
Other score of diagnosis agreement for the images interpretation by 3 physicians The agreement will be between conventional record and striatum focus record with VERITON camera 18 months
Other uptake ratios on the conventional record and on the focus brain record with VERITON the uptake ratios are:caudate nuclei/occipital cortex, putamen/occipital cortex, to the right and caudate nuclei/medium cingulate cortex, putamen/medium cingulate cortex to left, obtained with conventional camera and on the brain focus record with VERITON-CT camera after each SPECT/CT exams
Other quality scores of images from conventional camera and from VERITON (brain) 0= very bad quality and impossible to do a diagnosis, 1=bad quality and difficult diagnosis, 2= medium quality, 3 = good quality and 4= excellent quality immediately after SPECT-CT exams
Other recording activity in striatal area for the images from conventional camera and from VERITON (brain) recorded activities will be reported by injected MegaBecquerel (MBq) for the images obtained with the conventional camera and with VERITON brain focus record 18 months
Other diagnosis agreement for the interpretation by 3 physicians between conventional and VERITON (brain) The agreement will be between conventional record and brain focus record with VERITON camera 18 months
Primary Degree of concordance (Kappa) of the exams results of different records comparison between the exam results (positive diagnosis of Parkinson disease or Lewy bodies dementia versus differential diagnosis) in conventional camera and the one obtained with the VERITON-CT in striatum focus mode 16 months
Secondary Degree of concordance (Kappa) of the exams results of different recordings comparison between the exam results (positive diagnosis of Parkinson disease or Lewy bodies dementia versus differential diagnosis) in conventional camera and the one obtained with the VERITON-CT in brain focus mode 16 months
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