Comprehensive clinical evaluation of indirect bonding method in orthodontic treatment
Not Applicable
Recruiting
- Conditions
- Malocclusion
- Registration Number
- JPRN-UMIN000022182
- Lead Sponsor
- Okayama University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients with malocclusion 2)Patients with amelogenesis imperfecta or enamel hypoplasia 3)Patients with vomiting reflex 4)Patients with primary teeth 5)Patients with jaw deformity or syndrome 6)patients treated by minor tooth movement 7)Patients with poor oral hygiene 8)Patients who will not be able to continue the treatment until finishing the treatment 9)Inappropriate patients judged by principal investigator or members of this study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1) Treatment time (Months) 2) Comparison of occlusal index between pre-treatment and post-treatment (Scores) 3)Discomfort at the time of bonding (VAS score) 4)Oral hygiene after bonding (Plaque Control Record; %)
- Secondary Outcome Measures
Name Time Method 1) Chair time (Minutes) 2) Failure rate (Times)