- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06620718
Evaluation of Root Migration Distance After Coronectomy of Impacted Third Molars (NonRCT)
Evaluation of Pain and Root Migration Distance After Coronectomy Procedure of Impacted Third Molars Based on Age
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The roots of impacted lower third molars may be associated with the inferior alveolar nerve (IAN). To mitigate this risk and reduce trauma to the patient, a conservative approach involving the removal of the problematic crown portion and leaving the root may be adopted.
This clinical study was conducted between 2021-2022 years and was accordance with the Helsinki Declaration of 1975, as revised 2013. All subjects were informed about the study and clinical procedures and provided written consent The study included 73 patients aged between 18-55 years. These patients were divided into two age groups: The first group, consisting of patients aged 18-30. The second group, consisting of patients aged 31-55.
The coronectomy was surgically performed. Postoperative pain, swelling, and interincisal distance were evaluated based on age. Pain was assessed using a 10 cm Visual Analog Scale (VAS) with patients providing ratings before the operation and on the 3rd and 7th postoperative days. The progresion of endodontic lesion was evaluated in 6 months after coronectomy.
The distance of root migration achieved at 6 months after coronectomy was measured by independent examiner. Calibrated panoramic radiographs were used to determine the level of migration.
The statistical analysis of the data obtained in our study was performed using SPSS software The needed statistical analyses were used for comparison of the data. The Levene test was used for comparison of the root migration distances in the age groups. The significance level was set at 0.05.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Hatay, Turkey
- Hatay Mustafa Kemal University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
The study focused on applying coronectomy, a more conservative approach, instead of extraction for mandibular third molars associated with the inferior alveolar nerve that were indicated for prosthetic, orthodontic, prophylactic purposes, or those causing pericoronitis
- Systemically health,
- To maintain ideal oral hygiene,
- Absence of caries, pulpal and endodontic lesions in the impacted third molar indicated for extraction
- No known allergies to any antibiotics, or no use or history of bisphosphonate medication
- No use of tobacco or any illicit drugs by the patient.
- Not being pregnant
Exclusion Criteria:
- Other conditions unlike abovementioned items.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Evaluation of root migration at sixth month after coronectomy
Seventy three patients were divided into two age groups: The first group, consisting of patients aged 18-30, included 17 males and 23 females.
The second group, consisting of patients aged 31-55, included 17 males and 16 females
|
The inferior alveolar nerve and buccal nerve were blocked with maxicaine anaesthetic solution (articaine hydrochloride 40 mg, epinephrine hydrochloride 0.006 mg).
Incisions were applied uniformly across all patients, and a triangular flap technique was employed.
After elevating the flap and exposing the bone, the bone overlying the crown of the tooth was removed using a bone round bur to fully visualize the tooth's crown.
Once the crown was fully exposed, the crown preparation was initiated at the enamel-dentin junction using a fissure bur.
The crown preparation was completed without leaving any sharp edges, and the crown was extracted.
Then, the exposed pulp was washed with sterile serum without any further intervention.
The surgical area was sutured using 5/0 silk.
Analgesic (25 mg of dexketoprofen trometamol twice a day) and antibiotic (125 mg clavulanic acid, 875 mg amoxicilin twice a day) drugs were described.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the mesaurement of root migration distance
Time Frame: six months after coronectomy procedure
|
the distance from the enamel-cement line of the adjacent tooth to the remaining root or roots after coronectomy.
|
six months after coronectomy procedure
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the percentage of edema
Time Frame: postoperatively 3rd and 7th day after coronectomy
|
percentage of edema was measured extraorally
|
postoperatively 3rd and 7th day after coronectomy
|
|
the measurement of the distance of interincisal opening
Time Frame: postoperatively 3rd and 7th day after coronectomy
|
maximum interincisal distance was measured using a calliper during the maximum opening of the mouth
|
postoperatively 3rd and 7th day after coronectomy
|
|
the pain assessment
Time Frame: postoperatively 3rd and 7th day after coronectomy
|
A 10 cm or 100 mm-Visual Analogue Scale was used for assessment.
The findings suggested that 100-mm VAS ratings of 0 to 4 mm can be considered no pain; 5 to 44 mm, mild pain; 45 to 74 mm, moderate pain; and 75 to 100 mm, severe pain.
|
postoperatively 3rd and 7th day after coronectomy
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Osman F ARPAĞ, Mr, Mustafa Kemal University
Publications and helpful links
General Publications
- Ghaeminia H, Meijer GJ, Soehardi A, Borstlap WA, Mulder J, Berge SJ. Position of the impacted third molar in relation to the mandibular canal. Diagnostic accuracy of cone beam computed tomography compared with panoramic radiography. Int J Oral Maxillofac Surg. 2009 Sep;38(9):964-71. doi: 10.1016/j.ijom.2009.06.007. Epub 2009 Jul 28.
- Pedersen MH, Bak J, Matzen LH, Hartlev J, Bindslev J, Schou S, Norholt SE. Coronectomy of mandibular third molars: a clinical and radiological study of 231 cases with a mean follow-up period of 5.7years. Int J Oral Maxillofac Surg. 2018 Dec;47(12):1596-1603. doi: 10.1016/j.ijom.2018.06.006. Epub 2018 Jul 14.
- Hashemipour MA, Tahmasbi-Arashlow M, Fahimi-Hanzaei F. Incidence of impacted mandibular and maxillary third molars: a radiographic study in a Southeast Iran population. Med Oral Patol Oral Cir Bucal. 2013 Jan 1;18(1):e140-5. doi: 10.4317/medoral.18028.
- Satilmis T, Garip H, Arpaci E, Sener C, Goker K. Assessment of combined local anesthesia and ketamine for pain, swelling, and trismus after surgical extraction of third molars. J Oral Maxillofac Surg. 2009 Jun;67(6):1206-10. doi: 10.1016/j.joms.2008.12.034.
- Agbaje JO, Heijsters G, Salem AS, Van Slycke S, Schepers S, Politis C, Vrielinck L. Coronectomy of Deeply Impacted Lower Third Molar: Incidence of Outcomes and Complications after One Year Follow-Up. J Oral Maxillofac Res. 2015 Jun 30;6(2):e1. doi: 10.5037/jomr.2015.6201. eCollection 2015 Apr-Jun.
- Monaco G, de Santis G, Gatto MR, Corinaldesi G, Marchetti C. Coronectomy: a surgical option for impacted third molars in close proximity to the inferior alveolar nerve. J Am Dent Assoc. 2012 Apr;143(4):363-9. doi: 10.14219/jada.archive.2012.0178.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022/49
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Impacted Tooth With Abnormal Positioning
-
Damascus UniversityCompletedImpacted Tooth With Abnormal PositioningSyrian Arab Republic
-
Konya Necmettin Erbakan ÜniversitesiUnknownImpacted Third Molar Tooth | Periodontal Pocket | Impacted Teeth With Abnormal PositionTurkey
-
University of GenovaUniversity of MichiganCompletedComplicated Impacted ToothItaly
-
University of BaghdadRecruiting
-
esengul senCompletedImpacted Third Molar ToothTurkey (Türkiye)
-
Karamanoğlu Mehmetbey UniversityCompletedImpacted Third Molar ToothTurkey
-
Ankara UniversityCompletedImpacted Third Molar ToothTurkey
-
University of BaghdadCompletedImpacted Third Molar ToothIraq
-
zeynep cukurova yilmazCompletedImpacted Third Molar ToothTurkey
-
University of BaghdadCompletedImpacted Third Molar ToothIraq
Clinical Trials on coronectomy
-
The University of Hong KongCompletedPain | Infection | Alveolar Nerve InjuryChina
-
zeynep cukurova yilmazCompletedImpacted Third Molar ToothTurkey