Interest of the SPECT-CT Scan SUVspect in the New Generation of Gamma-cameras With Semiconductor
NCT ID: NCT03414021
Last Updated: 2024-03-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
250 participants
OBSERVATIONAL
2018-01-31
2025-12-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Until now, the interpretation criteria of scintigraphies are based on the homogeneity of distribution of a tracer in the explored organ (for single organs such as the heart or the thyroid, for example) or in the asymmetry of distribution of the tracer (for the double organs, such as the kidney or the joints).
This new gamma-camera allows to study the distribution of the radio-tracers in "list" mode, allowing to retrospectively reconstruct the images in various ways (for example, by modifying the size of the matrix of acquisition, the energy windows, the time of acquisition). Therefore, we can simulate and propose modifications in current procedures.
Every patient referred to our department of nuclear medicine to undergo a scintigraphy with a tracer of nuclear medicine (with a marketing authorization) can, while benefiting from an examination by this gamma-camera, to be the object of this study, and to profit from this additional information.
So, without changing the diagnosis or the usual care, we wish to take advantage of this additional information to improve the criteria of interpretation of our examinations.
This possibility being new, there is no available bibliography (our department is the 5th department of nuclear medicine in Europe to equip itself with this large field-of-view gamma-camera CZT, the DNM 670, made by General Electric), while 2961 articles speak about the SUVmax (in PET) in Pubmed.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Defining Dosimetric Reference Levels in Computed Tomography Spectral Scanning
NCT07305103
Relevance of Whole-body Computed Tomography Prescription in the Emergency Department : an Identification Tool for Low Risk Patients
NCT05588791
Data Collection Study for the Spectrum Dynamics Multi-purpose CZT SPECT Camera
NCT03438123
Low-dose Whole Body Computed Tomography Scanning
NCT03425032
Comparison of Imaging Quality Between Spectral Photon Counting Computed Tomography (SPCCT) and Dual Energy Computed Tomography (DECT)
NCT04328181
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Thyroid Diseases
SPECT-CT Scan
SPECT-CT Scan
Injection of a Tracer and SPECT-CT Scan
Heart Diseases
SPECT-CT Scan
SPECT-CT Scan
Injection of a Tracer and SPECT-CT Scan
Bone Diseases
SPECT-CT Scan
SPECT-CT Scan
Injection of a Tracer and SPECT-CT Scan
Brain Diseases
SPECT-CT Scan
SPECT-CT Scan
Injection of a Tracer and SPECT-CT Scan
Kidney Diseases
SPECT-CT Scan
SPECT-CT Scan
Injection of a Tracer and SPECT-CT Scan
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
SPECT-CT Scan
Injection of a Tracer and SPECT-CT Scan
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Patient under guardianship
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Lille Catholic University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tanguy Blaire, MD
Role: PRINCIPAL_INVESTIGATOR
GIE HUMANITEP, GHICL
Alban Baillez, MD
Role: PRINCIPAL_INVESTIGATOR
GIE HUMANITEP, GHICL
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hopital Privé Le Bois
Lille, Hauts-de-France, France
Humanitep
Lomme, Hauts-de-France, France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Tanguy Blaire, MD, PhD
Role: primary
Tanguy Blaire, MD, PhD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OBS-0030
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.