Skip to content

Application of Low-intensity Pulsed Ultrasound following genioplasty

Evaluation of efficacy of Low-intensity Pulsed Ultrasound on accelerating Mental nerve recovery following genioplasty

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241106063627N1
Enrollment
20
Registered
2024-12-08
Start date
2024-11-15
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Recovery of the mental nerve following genioplasty surgery.

Interventions

Intervention group: Low-intensity Pulsed Ultrasound applied on the treatment side by EXOGEN 4000+ device, Smith & Nephew Co., USA, on days 4, 8, 14 and 20 after surgery daily for 20 minutes with a dos

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who are candidates for genioplasty surgery.

Exclusion criteria

Exclusion criteria: Patients who have suffered trauma in the mandible area, especially in the chin area. Patients who have similar orthognathic surgery (SSO or Genioplasty) in the past. Patients who are candidates for orthognathic surgery along with genioplasty. During surgery, obvious nerve damage occurs or the nerve is not identified during surgery. Patients who use psychoactive drugs. Patients do not want to participate in the study. Patients who have suffered nerve damage due to other reasons in the past.

Design outcomes

Primary

MeasureTime frame
Two-point discrimination. Timepoint: Days 5, 9, 15 and 21 after surgery. Method of measurement: Millimetre.;Light touch. Timepoint: Days 5, 9, 15 and 21 after surgery. Method of measurement: Based on the patient's statement (positive or negative).;Low-intensity Pulsed Ultrasound (LIPUS). Timepoint: Days 4, 8, 14 and 20 after surgery. Method of measurement: MegaHertz, Milliwatt.;Thermal discrimination. Timepoint: Days 5, 9, 15 and 21 after surgery. Method of measurement: Centigrade.;Visual Analogue Scale (VAS). Timepoint: Days 5, 9, 15 and 21 after surgery. Method of measurement: Scoring from 0 to 10 (Based on the patient's statement).;Brush Test. Timepoint: Days 5, 9, 15 and 21 after surgery. Method of measurement: Determining the direction (positive or negative answer).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Shahoon

Shahed University

shahoonh@yahoo.com+98 21 8895 9210

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026