About this trial
This study tested whether low-intensity pulsed ultrasound (LIPUS) could help patients recover better after surgery to remove jaw cysts.
A total of 29 patients with 33 jaw cysts were included. After surgery, they were randomly assigned to two groups:
Ultrasound group (17 patients, 18 cysts): received daily LIPUS therapy for 10 days.
Control group (12 patients, 15 cysts): received the same care but with a sham (inactive) device.
The study was triple-blinded, meaning that the patients, the surgeon, and the evaluators did not know who was receiving real or sham treatment.
Researchers measured recovery in several ways:
Patient reports: pain, numbness, anxiety/depression, and oral health-related quality of life.
Clinician monitoring: checked for any side effects (like infection or burns). Imaging tests (CBCT scans): tracked how well bone healed by measuring changes in cyst cavity size (volume reduction) and new bone density.
All patients had the same type of surgery, performed by the same surgeon, and all provided written informed consent. The study followed international ethics and trial registration standards.
Eligibility criteria
Qualifiers
age ≥18 years.
having undergone cyst enucleation with curettage.
postoperative histopathological confirmation of a jaw cyst.
willingness to complete 10 days of standardized LIPUS therapy
Disqualifiers
severe psychiatric disorders impairing compliance.
acute infection.
presence of a cardiac pacemaker.
osteoporosis.
Trial design
Treatments tested in this trial
- Low-Intensity Pulsed Ultrasound