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Clinical Trials/NCT02071030
NCT02071030
Completed
Not Applicable

The Efficacy of Cone Beam Computed Tomography (CBCT) Compared to Panoramic Radiography Prior to Third Molar Removal; a Multicentre Randomised Controlled Trial

Radboud University Medical Center1 site in 1 country477 target enrollmentJune 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Inferior Alveolar Nerve Injury
Sponsor
Radboud University Medical Center
Enrollment
477
Locations
1
Primary Endpoint
Number of participants with inferior alveolar nerve (IAN) injury
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the efficacy and cost-effectiveness of Cone Beam Computed Tomography (CBCT) compared to panoramic radiography prior to removal of third molars in reducing patient's morbidity. Adults having a close relationship between the mandibular canal and one or both lower third molars, as diagnosed from digital panoramic radiographs will be recruited for this randomised controlled trial. In one trial arm, patients will receive the standard digital panoramic radiograph prior to third molar surgery. In the second arm, subjects will undergo an additional Cone Beam Computed Tomography (CBCT) prior to third molar surgery.

All patients require a postoperative visit one week after surgery to assess the outcome.

Registry
clinicaltrials.gov
Start Date
June 2013
End Date
June 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults \>18 year
  • mandibular canal is superimposed more than one half by the roots of the third molar as assessed on panoramic radiograph.

Exclusion Criteria

  • pregnancy
  • radiological evidence of cyst an tumors
  • indication for removal under general anesthesia
  • preoperative neurosensory alterations
  • existence of an external CBCT

Outcomes

Primary Outcomes

Number of participants with inferior alveolar nerve (IAN) injury

Time Frame: 1 week after surgery

Secondary Outcomes

  • Change in Oral Health related quality of life score(1 week after surgery)

Study Sites (1)

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