Can sound waves make jaw surgery safer and faster?
NCT ID NCT07730320
First seen Jul 28, 2026 · Last updated Jul 29, 2026 · Updated 1 time
Summary
This trial tests whether using a piezoelectric device (which uses ultrasonic vibrations) to cut bone during Le Fort I osteotomy reduces surgery time and blood loss compared to the conventional method using a mallet and chisel. The study includes 60 adults with old, improperly healed maxillary fractures who have not had prior treatment. Researchers will measure how long the surgery takes and how much blood is lost during the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- piezoelectric device (piezosurgery) compared with conventional mallet and osteotome
- What this could lead to
- If piezosurgery reduces surgery time and blood loss, it could become a preferred technique for correcting old maxillary fractures.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, so results may not apply broadly. Piezosurgery requires specialized equipment and training.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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Sep 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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15 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Malunited Lefort I Fracture of Maxilla for more than three weeks old * Untreated Maxillary Fractures. * Lefort I fracture on CT SCAN FACE with 3D reconstruction * Individuals with ASA1 and ASA2 Exclusion Criteria: * Previous Maxillofacial Treatment * Lactating mothers and Pregnant Females * Any Bone pathology or bone disease determined on Xray
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Allama Iqbal Medical College/Jinnah Hospital Lahore
Lahore, Punjab Province, 55400, Pakistan
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Other studies related to the condition(s) this trial covers.