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For Jaw Cysts/Jaw Tumors/Impacted Teeth Investigating the safety of optical navigation

For Jaw Cysts/Jaw Tumors/Impacted Teeth Investigation of the safety of optical navigation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs022250005
Enrollment
15
Registered
2025-05-23
Start date
2025-08-25
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign jawbone tumor/benign jawbone cyst/impacted teeth Benign jawbone tumor/benign jawbone cyst/impacted teeth

Interventions

To compare the safety and usefulness of the optical navigation technique with conventional methods and previous literature in 15 patients planning surgical treatment (jaw cystectomy/jaw tumor extracti

Sponsors

Morishima Hiromitsu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Persons who have given written consent to participate in the research (2) Patients diagnosed with benign jawbone tumor/benign jawbone cyst/impacted teeth (3) Patients who will undergo jawbone cystectomy/jawbone tumor removal/extraction of buried excessive teeth. (4) Those who are between 18 and 70 years of age (regardless of gender) at the time of obtaining the same (5) Persons with Performance Status 0-1

Exclusion criteria

Exclusion criteria: (1) Those whose crown prosthesis is expected to increase artifacts during cone-beam CT (CBCT) imaging. (2) Patients who have difficulty placing the X-clip in the mouth (3) Patients who are pregnant or lactating (4)Patients who have previously undergone conventional jaw cystectomy, jaw tumor extraction, or extraction of a buried tooth at the same site. (5) Patients who are deemed inappropriate for inclusion in the study by the principal investigator.

Design outcomes

Primary

MeasureTime frame
The adverse events and their rates of occurrence within one week after the procedure to which this method is applied will be compared with those of the conventional method. In consideration of the impact of differences in surgeons on the evaluation, comparisons should be limited to cases performed by surgeons with 10 or more years of experience in oral surgery.

Secondary

MeasureTime frame
The time required for surgery, especially for jaw shaping, will be compared with the time required for the conventional method. Surgical time is defined as the time from the start of surgery to the end of surgery. The time required for jaw shaping is defined as the time from the start to the end of the use of the rotary cutting instrument. In consideration of the impact of differences in surgeons on the evaluation, comparisons should be limited to cases performed by surgeons with 10 or more years of experience in oral surgery.

Contacts

Public ContactHiromitsu Morishima

Tohoku University Hospital

hiromitsu.morishima.b3@tohoku.ac.jp+81-22-717-8352

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026