An interventional study of wrist Cone-beam CT and wrist CT scan in Wrist Injuries and Ligament Injury, sponsored by Centre Hospitalier Universitaire de Besancon. Not yet recruiting. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-08.
Sponsored by Centre Hospitalier Universitaire de Besancon · Not applicable, Interventional, and Diagnostic
Recent advances in personalized 3D modeling make it possible to consider personalized hand modeling based on cone-beam CT. The goal is to develop a personalized 3D modeling tool for use in routine clinical practice that reduces both the radiation dose to which patients are currently exposed during CT scans and the time required to process CT data (segmentation). the main, objective of the study is to compare the quality of 3D hand modeling based on cone-beam CT with the gold standard of computed tomography.
This prospective, single-center, interventional study will include 6 healthy volunteers.
46 studies on the registry are indexed under Wrist Injuries; 12 are open to participants now.
This study's planned enrollment of 6 is below the median of 53 across 32 interventional studies indexed under Wrist Injuries.
Browse Wrist Injuries studies →Centre Hospitalier Universitaire de Besancon is the lead sponsor of 450 studies on the registry; 97 are open to participants now.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Contraindication
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
All subject will perform a wrist cone-beam CT 7 days after inclusion and a wrist CT scan 22 days after inclusion
Other: wrist Cone-beam CT · Other: wrist CT scan
Perfoming a wrist Cone-beam scan 7 days after study inclusion
Perfoming a wrist CT scan 22 days after study inclusion
To Estimate the mean bias (mm) and 95% confidence intervals between cone-beam CT and the gold standard (CT)
To compare the quality of 3D hand modeling based on cone-beam CT with the gold standard of computed tomography.
Time frame: 22 days after inclusion
No study locations are listed for this record.
Start is estimated for Jun 2026; primary completion for Oct 2026, 4 months later.
Of 17 interventional studies with no phase under Wrist Injuries, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 6 and three quarters within 58. This study's planned 4 months is below that.
How these figures are worked out, and which studies are left out of them.
This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.
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