rotation of teeth. Anomalies of tooth position
Conditions
Interventions
Intervention 1: Intervention 1 : Conventional fiberotomy :
After local anesthesia by injection of lidocaine 2% with epinephrine 1.100000 fiberotomy is done around the tooth to the alveolar socket by
Treatment - Surgery
Intervention 1 : Conventional fiberotomy :
After local anesthesia by injection of lidocaine 2% with epinephrine 1.100000 fiberotomy is done around the tooth to the alveolar socket by inserting the t
Intervention 2 : Erbium laser aided fiberotomy :
After local anesthesia by injection of lidocaine 2% with epinephrine 1.100000 fiberotomy is done around the tooth to the alveolar socket by inserting
Intervention 3 : Control : No type of fiberotomy is done really
Sponsors
vice chancellor for research and technology, Hamadan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
12 Years to 20 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria : Patients undergone orthodontic treatment who are 12-20 years old at the start of treatment and they are in finishing phase of active treatment with at least one rotated mandibular incisor before treatment ; Degree of rotation should be 20 to 70 degrees. Exclusion criteria : Patients with systemic diseases such as diabetes ; Patients with periodontal disease ; Patients with uncontrolled gingival inflammation (edema, bleeding on probing) ; Patients using osteoclast inhibitor medications ; Teeth with deep proximal caries extended to cemento enamel junction (CEJ) ; Teeth with developmental and anatomical malformations ; Teeth that were stripped during treatment.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Relapse. Timepoint: Two months after the intervention. Method of measurement: By measuring on the digitized dental models in degrees. | — |
Secondary
| Measure | Time frame |
|---|---|
| Dental clinic crown height in the facial surface. Timepoint: At the time of intervention , 2 months after the intervention. Method of measurement: Using a caliper in millimeter.;Probing depth around the tooth. Timepoint: At the time of intervention , 2 months after the intervention. Method of measurement: using a periodontal probe in millimeter.;Pain. Timepoint: 24 hours after intervention. Method of measurement: to answer the McGill Pain Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAmirfarhang Miresmaeili
Hamadan University of Medical Sciences
Outcome results
None listed