Clinical evaluation of custom-made brackets
- Conditions
- malocclusion
- Registration Number
- JPRN-jRCTs022230061
- Lead Sponsor
- Kanetaka Hiroyasu
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 26
(1) Patients who voluntarily consented in writing to participate in this clinical trial (parental authority for minors)
(2) Malocclusion (excluding skeletal malocclusion requiring orthodontic treatment) and no congenital anomalies.
(3) Male and Female between the ages of 13 and 30 at the time of informed consent
(4) Patients who are judged to have finished or about to finish pubertal growth. (Determined by X-rays of carpal bones, etc.)
(1) Jaw deformity patients and congenital syndrome patients
(2) Patients intended for stage I treatment
(3) Patients who have experienced orthodontic treatment
(4) Patients who are expected to have difficulty in continuing treatment at Tohoku University Hospital until the end of treatment
(5) Patients with vomiting reflex that makes impression taking difficult
(6) Female who are pregnant, may be pregnant, have given birth within 28 days, or are breastfeeding
(7) Patients who are considered difficult to participate in the study due to complication of psychosis or psychiatric symptoms
(8) In addition, patients who are judged to be inappropriate as subjects by the principal investigator or co-investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method