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Jaw surgery paste under scrutiny: does it raise infection risk?

NCT ID NCT02918344

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study followed 196 patients who had jaw-lengthening surgery to see if using a calcium phosphate paste leads to more infections or hardware removal. The paste is meant to prevent a visible notch and improve stability. The goal was to weigh these benefits against any added risks.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
calcium phosphate paste
What this could lead to
If successful, this could show that the paste safely improves jaw surgery outcomes by preventing notching and stabilizing bone segments.
What could go wrong
This is a completed observational study, not a treatment trial. It only compares complication rates, so it cannot prove the paste works better than standard care.

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.

Participants

196 people

The number who actually took part.

Started

Mar 2017

Finished

Apr 2020

Lead sponsor

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.

Who is studied

Patients undergoing bilateral sagittal split osteotomy

Ages

15 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: * All patients with dysgnatic deformities requiring mandibular lengthening surgery * Gender: M/F * Age: \>15y-75y Exclusion Criteria: * Previous orthognathic surgery * Congenital facial malformations * Unilateral SSO * Immunodeficiency * Simultaneous removal of lower third molars * Incomplete postoperative follow-up

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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

  • universitair Ziekenhuis brussel

    Jette, Brussels Capital, 1090, Belgium

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Other studies related to the condition(s) this trial covers.