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Evaluation of the Mental Foramen After Surgery Via Ultrasonography

Evaluation of Changes in Mental Foramen Blood Flow After Orthognathic Surgery Using Ultrasound

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06661798
Acronym
Blood flow
Enrollment
16
Registered
2024-10-28
Start date
2024-10-01
Completion date
2025-03-28
Last updated
2025-07-15

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

Conditions

Orthognathic Surgery

Keywords

Mental foramen, orthognathic surgery, blood flow, ultrasonography

Brief summary

Objective: This study aims to detect changes in blood flow in the mental foramen after surgery compared to before orthognathic surgery. Materials and Methods: This study will include a total of 16 patients, aged between 18-60, who were planned for orthognathic surgery due to malocclusion complaints. Patients will be evaluated clinically and radiologically before surgery, 1 week, 1 month, and 3 months after the surgery. Panoramic radiographs will be taken before surgery and 3 months after surgery, and a fractal analysis of the ROI area determined distal to the mental foramen will be performed. Pain will be scored from 1 to 5 using the Pinprick test before surgery, 1 week, 1 month, and 3 months after surgery, while pressure and neurosensitivity will be scored using VAS. Neurosensory evaluation will be performed using two-point discrimination (dividing the area between the lower lip and chin into 9 regions), and left-right discrimination will be checked using the brush test. Blood flow in the mental foramen will be evaluated using ultrasonography.

Interventions

PROCEDUREorthognathic surgery

Mandibular setback, Maxillary advancement, Bilateral sagital split osteotomy

PROCEDUREUSG examination

Comparison of blood flow in the mental foramen before and 1week, 1 month and 3 month after orthognathic surgery using ultrasound examination

PROCEDURESubjective evaluation - Neuro-sensitivity tests

Direction determination, two-point separation, pinprick, and brush tests, along with neurosensitivity VAS and pressure VAS, were applied to the patients. These tests were performed before surgery (T0), seven days after surgery (T1), one month after surgery (T2), and three months after surgery (T3).

Sponsors

Bezmialem Vakif University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

1. Patients over 18 years old, 2. Patients who have reached skeletal maturity, 3. Patients under 60 years old, 4. Patients with skeletal Class II malocclusion indicated for orthognathic surgery, 5. Patients with skeletal Class III malocclusion indicated for orthognathic surgery, 6. Those who are willing to participate in the study

Exclusion criteria

1. Patients with a systemic disease, 2. Patients under 18 years old, 3. Patients who have not completed their growth and development, 4. Patients over 59 years old, 5. Patients using neurological and psychiatric medications, 6. Patients who have previously undergone surgery or experienced trauma in the mandibular region, 7. Patients with neurosensory dysfunction in the inferior alveolar nerve before surgery, 8. Pregnant individuals or those suspected of being pregnant, 9. Any local or systemic condition that may contraindicate general anesthesia

Design outcomes

Primary

MeasureTime frame
Changes in blood flow in the mental foramen after orthognathic surgeryFrom enrollment to 3 months after the end of surgery

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026