Bone Height and Extractions Study

NCT ID: NCT03909568

Last Updated: 2019-10-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-30

Study Completion Date

2021-08-31

Brief Summary

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A coronectomy is often chosen over complete extraction of a lower third molar when the tooth appears to be in close proximity to the inferior dental (ID) canal, as assessed on a plain radiograph or a cone beam computer tomograph (CBCT). Following a coronectomy, the roots of the third molar may migrate in a coronal direction. This effect, along with the bone-preserving technique of a coronectomy over extraction, may provide increased bone height distal to the lower second molars, when compared to extraction. Partially erupted lower third molars, specifically those with mesio-angular impactions, are commonly associated with reduced bone height distal to lower second molars, and cause damage to the periodontal support of these neighboring teeth. It is assumed that maintenance of the impacted third molars or extraction of these teeth may compromise the periodontal status of the lower second molars. This study will investigate if coronectomy improves the bone levels, and therefore the periodontal status, of lower second molars, and may propose an indication for a coronectomy regardless of the proximity of the tooth to the ID canal.

Coronectomies were first proposed as a treatment option just over thirty years ago, but there are very few long-term studies on the procedure reported in the literature. To the best of the investigator's knowledge, this will be the first randomised controlled trial comparing the bone height distal to the lower second molar following a coronectomy or extraction of the lower third molar.

Detailed Description

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Conditions

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Alveolar Bone Loss Periodontal Attachment Loss Periodontal Pocket

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Split-mouth
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Patients will be initially masked to which treatment is performed on each side, but will be notified at the follow-up appointment. In addition, the outcomes assessor carrying out the periodontal measurements (clinical attachment level and probing depths), will be unaware which treatment will be performed. The same surgical flap designs will be used for the treatment of both the right and left third molars, regardless of whether a coronectomy or extraction is carried out, and therefore the patient and clinician should be unable to differentiate between the procedures performed. Intervention will only be revealed to care provider once surgical flaps have been raised.

Study Groups

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Third molar surgery

Split mouth comparison of effect of complete third molar removal vs coronectomy of contralateral third molar

Group Type EXPERIMENTAL

Third molar surgery

Intervention Type PROCEDURE

Comparing complete removal of third molar with removal of crown only on contralateral side

Interventions

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Third molar surgery

Comparing complete removal of third molar with removal of crown only on contralateral side

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients requiring extraction of both lower third molars
* Both lower third molars to have mesio-angular impa
* ctions, as assessed by location of the contact point between the crown of the third molar and the cemento-enamel junction (CEJ) of the second molar and the angulation of the third molar
* Both lower third molars must lie above or clear of the ID canal as assessed on a plain radiograph or CBCT
* Presence of lower second molars
* Patients must be ≥18yrs old
* Patients willing to attend follow up appointments

Exclusion Criteria

* Lower third molars with caries, periapical pathology or associated lesions such as cysts
* Patients who are immunocompromised, have a history of or due to have head and neck radiotherapy, chemotherapy, have previously been given or due to start intravenous bisphosphonates
* Smokers (\>5 cigarettes/day)
* Patients involved in current research or have recently been involved with research prior to recruitment
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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King's College London

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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249253

Identifier Type: -

Identifier Source: org_study_id

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