MedPath

sefulness of intraoperative image support system in orthognatic surgery

Phase 1
Not yet recruiting
Conditions
Jaw deformity
aw deformity
Registration Number
JPRN-jRCT1032220599
Lead Sponsor
Shirota Tatsuo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

1) Clinical diagnostic criteria for jaw deformity in patients admitted to or outpatients at the Department of Maxillofacial and Maxillofacial Surgery, Showa University Dental Hospital
Patients who meet
2)Patients scheduled to undergo surgery for jaw deformity using an intraoperative image support system at our hospital.
3) Patients aged between 18 and 60 at the time of informed consent.
4) Patients who have completed preoperative orthodontic treatment by the time consent is obtained.
5)Patients who gave their written informed consent to participate in this study. If the applicant is under 20 years of age, written consent must be obtained from the legal representative.

Exclusion Criteria

1) When there is a request for discontinuation from the subject (or legally acceptable person)
2) If the study is interrupted due to the subject's circumstances (move, change doctor/hospital, busy schedule, loss of follow-up, etc.)
3) When it turns out that the subject is not a target case after the start of the study
4) In the event of an accidental accident
5) When an adverse event occurs (including aggravation of the primary disease, aggravation of complications or complications) and the investigator judges that the study should be discontinued
6) When it becomes difficult to continue the study due to insufficient effect or worsening of symptoms
7) If there is a serious deviation from this study protocol and it is judged that it cannot be evaluated
8) When it turns out that the subject did not take the medicine as instructed by the investigator
9) In addition, if the investigator judges that it is difficult to continue the study and it is appropriate to discontinue the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath