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Safety of Coronectomy vs Excision of Wisdom Teeth (coronrct)
This study has been completed.
Sponsored by: The University of Hong Kong
Information provided by: The University of Hong Kong
ClinicalTrials.gov Identifier: NCT00752284
  Purpose

The purpose of this study is to compare the surgical complications and neurosensory disturbance of coronectomy and conventional excision of wisdom teeth with roots in close proximity to inferior alveolar nerve. Hypothesis: Coronectomy of wisdom tooth can reduce the chance of injury to the inferior alveolar nerve in cases of radiographic proximity to the roots when compared with conventional method of surgical removal of wisdom teeth, and there is no difference in other surgical morbidities.


Condition Intervention
Pain
Infection
Alveolar Nerve Injury
Procedure: Coronectomy
Procedure: Total Excision

U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Active Control, Parallel Assignment, Safety Study
Official Title: Randomized Controlled Trial of Safety of Coronectomy Versus Excision of Wisdom Teeth

Further study details as provided by The University of Hong Kong:

Primary Outcome Measures:
  • The incidence of neurosensory disturbance, infection or dry socket of control group and coronectomy group [ Time Frame: 1 week-2 years ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Migration rate of root in coronectomy group [ Time Frame: 1 week - 2 years ] [ Designated as safety issue: No ]

Enrollment: 349
Study Start Date: June 2006
Study Completion Date: August 2008
Primary Completion Date: August 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
A: Experimental
Coronectomy Group. Removal of crown of lower wisdom tooth, trim down root below crestal bone and primary closure
Procedure: Coronectomy
Coronectomy Group. Removal of crown of lower wisdom tooth, trim down root below crestal bone and primary closure
B: Active Comparator

Control Group:

total excision of lower wisdom tooth

Procedure: Total Excision
Total excision of lower third molar

Detailed Description:

Complications of impacted wisdom teeth, such as pericoronitis, caries and periodontal disease are common, and these contribute to the indications that third molar surgery is still the most common oral surgical procedure performed. Damages to the inferior alveolar nerve (IAN) during surgical removal of deeply impacted wisdom teeth is a well-known complication. Over the years, reports of IAN deficit after wisdom teeth surgery were recorded from 0.4% to 8.4%. Injury to IAN can be due to compression of the nerve, either by indirect force transmitted by the root during elevation or directly by elevators. It is also possible for the nerve to be transected causing neurotmesis by rotary instruments or when the tooth is grooved or perforated by IAN. Several studies have tried to correlate radiographic markers and relationship of IAN and the root of wisdom teeth. Howe and Poyton identified 3 radiographical signs that the roots of wisdom teeth maybe grooved, notched, or perforated by the IAN 2. Rood and Shehab in 1990 suggested diversion of the canal, darkening of the root and interruption of the white line of IAN to be significantly related to IAN injury. Sedaghatfar et al. in 2005 performed a retrospective cohort study and confirmed that, and adding to it narrowing of the root to be an additional significant sign to predict the proximity of nerve and root. These radiographic signs only indicate to surgeons and patients that there is an increased risk of nerve damage associated with the removal of the corresponding wisdom tooth, but not a prevention to it if the tooth is being removed.

Coronectomy is a procedure intentionally aiming to remove only the crown of an impacted mandibular third molar, leaving the root undisturbed, and thus avoiding possible direct or indirect damage to the IAN. This technique was first described by Knutsson et al. in 1989 in a retrospective study of 33 patients. 6 more papers about coronectomy were published to date, with 3 case reports and 2 retrospective studies, and one randomized controlled trial by Renton et al. in 2005.In this last study, 128 patients were randomized to undergo either extraction or coronectomy of wisdom teeth. The group undergoing extraction was found to be significantly more common in experiencing IAN deficit after surgery than the coronectomy group, while no significant differences could be concluded in terms of other surgical morbidities. The other studies also drew similar conclusions. One common finding, however, was the slow superficial migration of the wisdom tooth root after coronectomy. It had been suggested the root is only indicated to be removed only if it is exposed intraorally, but the risk of IAN damage of the second surgery is reduced as the root has migrated away from the nerve.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Radiographically the wisdom tooth root is touching or overlapping with the superior cortical line of inferior alveolar nerve or showing one or more of the following signs:

    • darkening of root
    • abrupt narrowing of root
    • interruption and loss of the white line of IAN canal
    • displacement of the IAN canal by the roots
    • Abrupt narrowing of one or both of the canal white lin

Exclusion Criteria:

  • Wisdom tooth roots not touching the IAN cortical lines
  • Wisdom tooth presented with apical pathology
  • Pre-existing neurosensory deficit of IAN
  • Systemic condition predisposing local infection: diabetes, AIDS, concurrent chemotherapy.
  • Local factors predisposing infection: metabolic bone diseases e.g. fibrous dysplasia, history of radiotherapy on mandible
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00752284

Locations
China
Prince Philip Dental Hospital
Hong Kong, China
Sponsors and Collaborators
The University of Hong Kong
Investigators
Principal Investigator: Yiu Yan Leung, BDS U Hong Kong
Study Director: Lim Kwong Cheung, BDS, PhD U Hong Kong
  More Information

Responsible Party: Oral and maxillofacial surgery, the Univeristy of Hong Kong ( Dr Yiu Yan Leung )
Study ID Numbers: UW 06-218 T/1243
Study First Received: September 1, 2008
Last Updated: December 5, 2008
ClinicalTrials.gov Identifier: NCT00752284  
Health Authority: Hong Kong: Ethics Committee

Keywords provided by The University of Hong Kong:
coronectomy
neurosensory deficit
third molar surgery

Study placed in the following topic categories:
Pain

Additional relevant MeSH terms:
Infection

ClinicalTrials.gov processed this record on January 16, 2009