Study on the Risk of Inferior Alveolar Nerve Damage During Lower Third Molar Surgery

Sponsor
University of Roma La Sapienza (Other)
Overall Status
Completed
CT.gov ID
NCT04807946
Collaborator
(none)
92
34.3

Study Details

Study Description

Brief Summary

Objective The present study aimed to evaluate which factors were statistically associated with a greater probability of inferior alveolar nerve (IAN) damage during lower third molar surgery.

Study Design A prospective observational study was performed at the Oral Surgery Unit of the Umberto I Hospital on 92 patients which underwent surgical extraction of a lower third molar, that was radiographically overlapped to the mandibular canal. All surgeries were performed by the same expert surgeon. A principal component analysis and the exact two-tailed Fisher test were used.

Condition or Disease Intervention/Treatment Phase
  • Procedure: lower third molar extraction

Detailed Description

Exclusion criteria were the following:
  • lower third molar buds;

  • lack of contiguous second molar;

  • wide cyst-like areas or severe osteo-metabolic/tumor pathologies associated with the lower third molar;

  • pre-operative neurosensory deficit related to IAN on the side where surgery was to be performed.

Clinical and radiographic data were noted on a special chart, developed in four areas concerning the patient's personal data, pre-operative case evaluation, surgical technique, and post-operative course.

Assessment of surgical difficulty was reached using a modified Pederson's scale by assigning a 1 to 3 score to each of the following variables: tooth inclination (mesioangular/vertical = 1; horizontal = 2; distoangular = 3), depth of impaction (modified Winter classification: A/B = 1; C1 = 2; C 2= 3), Pell & Gregory class (I = 1; II = 2; III = 3), root morphology (fused or slightly divergent = 1; strongly divergent = 2; presence of apical anomalies = 3), proximity to the IAN (none = 1; contiguity = 2; embrication = 3) and maximum mouth opening (> 4 cm = 1; 3-4 cm = 2; < 3 cm = 3). For each extracted third molar, a total score between 6 and 18 was therefore obtained.

All surgeries were performed by the same expert surgeon (RP), with the buccal approach using local anesthesia, and included the following maneuvers:

  • luxation of the coronal portion of the tooth/root in an ipsilateral or parallel direction with respect to the IAN position and running, in order to minimize nerve compression;

  • post-extraction residual bone cavity inspection using a Zeiss 4x300 magnification optical system to better identify intra-operative nerve exposure.

No material was inserted into the residual cavity, neither by regeneration nor by haemostasis.

After one week, sensitivity was tested on both sides with the tactile test using a 27-gauge needle tip and, if a difference was found, the patient was followed up once a week for the first month and every two weeks thereafter, until he/she reported to perceive the pin-prick test in the affected side the same way as the healthy side.

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
92 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Prospective Observational Study on the Variables Affecting the Risk of Inferior Alveolar Nerve Damage During Lower Third Molar Surgery With Nerve/Root Proximity
Actual Study Start Date :
Apr 1, 2016
Actual Primary Completion Date :
Jan 29, 2019
Actual Study Completion Date :
Feb 8, 2019

Outcome Measures

Primary Outcome Measures

  1. Assessment of sensitivity alteration after extraction [After 7 days, at the suture removal, the sensitivity was tested.]

    sensitivity in the territory of innervation of the inferior alveolar nerve, sensitivity was tested on both sides with the tactile test using a 27-gauge needle tip and, if a difference was found, the patient was followed up once a week for the first month and every two weeks thereafter, until he/she reported to perceive the pin-prick test in the affected side the same way as the healthy side.

  2. Change of Sensitivity after every week for the first month [in case of alteration the checks were carried out every weeks up to 30 days]

    sensitivity in the territory of innervation of the inferior alveolar nerve, sensitivity was tested on both sides with the tactile test using a 27-gauge needle tip and, if a difference was found, the patient was followed up once a week for the first month and every two weeks thereafter, until he/she reported to perceive the pin-prick test in the affected side the same way as the healthy side.

  3. Change of Sensitivity after every two week for the second month until resolution [in case of alteration over 30 days we checks every 2 weeks until resolution, up to 365 days.]

    sensitivity in the territory of innervation of the inferior alveolar nerve, sensitivity was tested on both sides with the tactile test using a 27-gauge needle tip and, if a difference was found, the patient was followed up once a week for the first month and every two weeks thereafter, until he/she reported to perceive the pin-prick test in the affected side the same way as the healthy side.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • orthopantomographic superimposition between the lower third molar and at least the upper half of the mandibular canal, associated or not with the presence of one or more radiographic signs of proximity among those proposed by Rood and Shehab (1990):

  • 3-dimensional radiographic examination with a CT software;

  • any type of lower third molar impaction.

Exclusion Criteria:
  • lower third molar buds;

  • lack of contiguous second molar;

  • wide cyst-like areas or severe osteo-metabolic/tumor pathologies associated with the lower third molar;

  • pre-operative neurosensory deficit related to IAN on the side where surgery was to be performed.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Roma La Sapienza

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pippi Roberto, Professor, University of Roma La Sapienza
ClinicalTrials.gov Identifier:
NCT04807946
Other Study ID Numbers:
  • 4111
First Posted:
Mar 19, 2021
Last Update Posted:
Mar 19, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 19, 2021