RecruitingACTRN12610000638033

A prospective randomised comparative study on the use of panoramic radiograph and cone beam scan with respect to the outcomes and incidence of inferior alveolar nerve injury after lower third molar removal, and establishing guidelines for the indications of cone beam scan as an adjunct to panoramic radiographs

A prospective randomised comparative study on the use of panoramic radiograph and cone beam scan with respect to the outcomes and incidence of inferior alveolar nerve injury after lower third molar removal, and establishing guidelines for the indications of cone beam scan as an adjunct to panoramic radiographs in patients with impacted lower third molars


Sponsor

Royal Dental Hospital Melbourne

Enrollment

4,000 participants

Start Date

Nov 1, 2009

Study Type

Interventional

Conditions

Summary

A known risk factor for lower wisdom teeth removal is inferior alveolar nerve injury, due to the anatomical position and relationship of these two structures. Patients who are referred for wisdom teeth removal routinely have an orthopantomogram for preoperative assessment of these teeth. Cone beam scan, which is a low dose computed tomography scan providing 3-dimension representation of the site, is becoming increasingly popular for inferior alveolar nerve localization. However, there are no studies to show that additional scanning improves outcomes and decreases risk of post-operative numbness for the patient. Furthermore, there are currently no guidelines regarding clear indications for the use of cone beam scan as an adjunct. This project will look at the incidence of postoperative altered inferior alveolar nerve sensation in patients who have lower wisdom teeth removed – in groups where they have the routine orthopantomogram radiograph only, and those who have, in addition to the orthopantomogram radiograph, a cone beam scan. The project will aim to establish evidence based guidelines for the use of Cone beam scan imaging as an adjunctive tool for third molar surgery. Patients who agree to take part in the project will be randomised into two groups – the control is the group without additional imaging ("orthopantomogram only" group), and the intervention group is the group with the additional cone beam scan ("orthopantomogram and Cone beam scan" group). The imaging will be examined with respect to the relationship between the inferior alveolar nerve and lower wisdom teeth. During routine post-operative visits, patients are routinely monitored to establish the presence of inferior alveolar nerve injury. This data will be collected and analysed.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 50 Yearss

Plain Language Summary

Simplified for easier understanding

This study is comparing two types of imaging done before wisdom tooth removal to see which leads to better outcomes. Currently, all patients get a panoramic X-ray (called an OPG). Some patients may also get a cone beam CT scan — a 3D, low-dose scan that shows where the nerve is in relation to the tooth. Researchers want to find out if the extra scan actually reduces the risk of nerve injury after the procedure. You may be eligible if: - You are between 18 and 50 years old - You need to have your lower wisdom teeth removed - You are willing to consent to participate in the study You may NOT be eligible if: - You are pregnant - You are unable to give consent - You have jaw pathology or pre-existing numbness in the area - Your X-ray shows the nerve is more than 5mm away from the wisdom tooth Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

Patients participating in study (patients for lower wisdom teeth removal) will be randomised into two groups: 1- OPG (orthopantomogram) only as the preoperative imaging(gold standard) 2- OPG (orthop

Patients participating in study (patients for lower wisdom teeth removal) will be randomised into two groups: 1- OPG (orthopantomogram) only as the preoperative imaging(gold standard) 2- OPG (orthopantomogram) and cone beam scan as the preoperative imaging The intervention is: requesting an additional scan (Cone Beam Scan) of the third molar area The duration of intervention is approximately 5-10 mins (ie the duration to set up and take a cone beam scan is ~5-10mins) - ONLY one scan ie one session. Period of follow up is as per standard protocol for postoperative wisdom teeth follow up, that is: at 2 weeks postoperatively, if any concerns then at 3-4 weeks postop, if residual paraesthsia then 3months postop, then at 6months postop. If no paraesthesia and no problems after 2 weeks then patients are discharged.


Locations(1)

Australia

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ACTRN12610000638033