JPRN-jRCTs022230061
Not yet recruiting
Phase 1
An open-label, randomized controlled trial investigating the effect of shortening the duration of orthodontic treatment using a custom-made bracket system
Kanetaka Hiroyasu0 sites26 target enrollmentFebruary 21, 2024
Conditionsmalocclusion
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- malocclusion
- Sponsor
- Kanetaka Hiroyasu
- Enrollment
- 26
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(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.)
Exclusion Criteria
- •(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
Outcomes
Primary Outcomes
Not specified
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