The Impact of 3D-CBCT Imaging on Nerve Injuries During Wisdom Tooth Surgery
Launched by UNIVERSITY OF ABERDEEN · Feb 7, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying whether using a special 3D scan of the jaw can help reduce the risk of nerve injuries during wisdom tooth surgery. Nerve injuries can lead to problems like pain, tingling, or numbness in the lip, chin, and tongue, making it difficult to eat or speak. Currently, doctors use traditional 2D X-rays to see the position of the nerves and teeth, but it's not clear whether these images are as effective as 3D scans in preventing nerve damage.
To participate in this trial, you need to be at least 16 years old and have a wisdom tooth that needs to be surgically removed. You should also be able to consent to participate in the study and understand English well enough to read the information and answer follow-up questions. If you decide to join, you can expect to receive either a 2D or 3D scan before your surgery, and a follow-up call one week later to check on your recovery. This trial is currently looking for volunteers, and your participation could help improve the safety of future wisdom tooth surgeries.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Individuals are seen in the Oral Surgery department with a 2D-OPG x-ray and a diagnosis of a mandibular wisdom tooth that requires surgical treatment.
- • 2. Individuals requiring a 3D-CBCT to further assess the relationship between the wisdom tooth and the inferior alveolar nerve.
- • 3. Individuals who are to undergo surgical treatment for their wisdom tooth regardless of the surgical approach (e.g. coronectomy or extraction) or the anaesthetic technique utilised.
- • 4. Individuals without any pre-existing neurological deficit of cranial nerve V (trigeminal nerve) or medical conditions or medications that may cause changes in neurosensory function.
- • 5. Individuals over the age of 16 and willing and able to provide valid informed consent for themselves.
- • 6. Individuals with adequate English comprehension to read the written PIS and consent form and understand the follow-up call questions.
- • 7. Individuals willing to provide contact details to allow a telephone follow-up call one week after their surgery.
- Exclusion Criteria:
- • 1. Individuals who do not have the capacity to consent for themselves.
- • 2. Individuals taking medicines or having medical conditions and disorders that impair neurosensory function.
- • 3. Individuals requiring wisdom tooth surgery to manage associated pathology such as cysts, fractures, or tumours where the pathological condition may interfere with the neurosensory function of the trigeminal nerve at 1 week post-operatively.
- • 4. Individuals who are unable to read or speak English.
About University Of Aberdeen
The University of Aberdeen, a prestigious institution founded in 1495, is a leading center for research and education in healthcare and clinical sciences. With a commitment to advancing knowledge and improving patient outcomes, the university actively sponsors clinical trials that explore innovative treatments and therapies across various medical fields. Leveraging its interdisciplinary expertise and state-of-the-art facilities, the University of Aberdeen fosters collaborations with healthcare professionals and industry partners to enhance the quality of clinical research and contribute to the global medical community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
London, England, United Kingdom
Aberdeen, Scotland, United Kingdom
Aberdeen, Scotland, United Kingdom
Patients applied
Trial Officials
Anand Lalli, BDS PhD
Study Chair
Institute of Dentistry, University of Aberdeen
Rahmeh Alhyari, BDS MFDS RCSEd
Study Director
Institute of Dentistry, University of Aberdeen
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported