Traditional vs. orthodontic extraction of impacted teeth related to the inferior alveolar nerve: a randomized control trial
- PMID: 40604669
- PMCID: PMC12224594
- DOI: 10.1186/s12903-025-06402-7
Traditional vs. orthodontic extraction of impacted teeth related to the inferior alveolar nerve: a randomized control trial
Abstract
Background: The aim of this prospective randomized controlled trial was to compare the effects of orthodontic and traditional extraction methods on nerve injury following the extraction of impacted third molars close to the inferior alveolar nerve and to demonstrate the impact of factors such as gender, age, systemic diseases, the side of the third molar, its position, and classification on nerve recovery.
Methods: Patients with impacted third molars close to the inferior alveolar nerve and an indication for impacted third molar extraction were included in the study. The patients were divided into two groups according to the surgical approach to be applied.
Results: Preoperative 2-point discrimination (2PD) test values, as well as postoperative 2PD test and visual analog scales (VAS) values on the 7th day, 14th day, and 1st, 3rd, and 6th months, were compared. In the traditional extraction group, the results of the 2PD test were statistically significantly higher on the 7th day, 14th day, 1 month, and 3 months compared to the orthodontic extraction group (P < 0.05). Sex, age, systemic disease, M3 side, position, and classification had no statistically significant effect on nerve recovery (P > 0.05).
Conclusions: The orthodontic extraction was found to be safer than traditional extraction in terms of nerve injury for high-risk M3s.
Clinical trial registration: This study was registered on www.
Clinicaltrials: govin13/02/2024 .
Clinical trial number: NCT06270784.
Keywords: Impacted tooth; Inferior alveolar nerve; Mandibular nerve injuries; Orthodontic extrusion; Third molar; Tooth extraction.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: The present study was performed according to the guidelines of the Helsinki Declaration and complied with the CONSORT guidelines. Ethical approval was obtained from Marmara University Faculty of Medicine Clinical Research Ethical Commitee (IRB Approval No. 09.2024.122). Every patient signed a written informed consent form. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
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