Magnetic Resonance Imaging
OtherParticipants will receive an additional MRI image in addition to standard of care to investigate if it was a useful imaging modality for their condition
Not Yet Recruiting
NCT Number: NCT07008014
Can Dental Dedicated MRI Replace Low-dose CBCT Scanning in Dentistry
Magnetic Resonance Imaging (MRI) has is a useful diagnostic tool that offers advantages over conventional radiography techniques. Unlike traditional X-ray or computed tomography (CT) scans, MRI utilizes a magnetic field and radio waves to generate detailed and high-resolution images of the body's internal structures. This non-invasive imaging modality allows the clinician to better see soft tissues in 3D without the use of ionising radiation. Furthermore, MRI enables the detection and characterization of a wide range of pathologies which can lead to improved diagnostic capabilities and better patient outcomes.
To date, the use of MRI in dentistry has been limited as dentistry imaging focuses predominantly on hard tissues (teeth and bones) in addition to the higher cost and accessibility issues with MRI machines.
However, recent developments have led to the development of a dental-specific coil for use with a low field strength (0.55 Tesla) MRI scanner. This has resulted in high diagnostic quality soft and hard tissue images and reduced imaging time. As this imaging modality has rarely been used before in dentistry, the aim of this study is to investigate its use for dental imaging, refining parameters and assessing the diagnostic quality of dental scans taken using MRI and the specific dental coil.
Not Yet Recruiting
Trial opening soon.
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Conditions
Age range
3 year and older
Sex eligibility
All sexes
Study type
Observational
About this study
The overall aim of this feasibility project is to optimise MRI parameters for dental use (i.e., dental-dedicated MRI) and assess the diagnostic quality of dental scans taken using MRI.
The objectives are to assess if MRI imaging has altered the diagnosis, retrospectively analyse the numbers of patients which can be diagnosed effectively using this radiation free imaging modality and document health resource use to inform a full health technology assessment trial.
The primary objective is to assess the feasibility of providing MRI scanning to dental patients and the resultant benefit. As such, the investigators will examine the percentage of patients whose diagnosis was altered as a result of additional MRI scanning.
The secondary objectives are to assess:
- The percentage of patients who would have been able to complete their diagnosis with an MRI scan alone
- Percentage of eligible patients who agreed to have an MRI scan
- Percentage of patients who completed the MRI scan
- Clinician rated diagnostic acceptability
- Patient acceptability of the imaging modality (as determined by VAS scale)
- Documentation of Health resource use including intervention costs
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients aged 3 or over with suspected orofacial pathology involving a soft tissue component or healthy volunteers
- The patient is willing to undergo an MRI investigation
- Patient or their carer/guardian is able to provide informed consent to the study
Exclusion criteria
- Patient or their carer is unable to show Gillick competency for consent.
- The patient has pronounced claustrophobia.
- The patient has a pacemaker or implanted defibrillator.
- The patient has history of metal shrapnel injuries to the eyes or MRI incompatible metallic inclusions or implants/ large tattoos.
- The patient has non-removable piercings.
- Pregnant patients, or patients who suspect they could be pregnant
- The patient has participated in other research studies within the previous 30 days.
Treatment and study plan
Primary outcomes
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Percentage of patients whose diagnosis/care changed as a result of the additional dental MRI imaging compared to the total number of patients imaged using conventional radiography.
Time frame: 4 weeks
The treatment plan that was given before the MRI scan will be documented. Following review of the MRI by the overseeing consultant, any changes to the treatment plan will be documented. The number of patients whose treatment plan was altered as a result of the scan will be divided by the number of those who received a scan to get a percentage.
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To assess diagnostic quality of the image
Time frame: 6 months
This is a feasibility trial and a new imaging modality for dentistry. Working with MR physicists we will assess image quality and report on areas for improvement
Secondary outcomes
-
Percentage of patients whereby the diagnosis could have been obtained using dental-dedicated MRI alone
Time frame: 4 weeks
The number of patients whereby the clinical indicators of pathology on the MRI scan were sufficient to gauge the pathology will be assessed. This will be divided by the number of patients who received a scan to get a percentage.
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Time spent undergoing scan
Time frame: 4 weeks
Time spent undergoing scan (minutes)
-
Radiation exposure (Grays)
Time frame: 4 weeks
Radiation exposure of the imaging modality (Grays)
Study contacts
Contact information is provided by the study sponsor or research team.
Jonathan Consultant Maxillofacial Radiologist
CONTACT
Saoirse O'Toole, BDentSc PhD
CONTACT
Sponsors and collaborators
Lead sponsor
King's College London
Other
Registry information
Official study title
What is the Scope for Low Field MRI to Replace Cone Beam Computed Tomography in Dentistry?
Acronym: DDMRI
Important dates
- Study start
- 2025
- Primary completion
- 2025
- Study completion
- 2025
- First posted
- Jun 6, 2025
- Registry last updated
- Jun 29, 2025
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.