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Custom 3D-Printed titanium implants could rebuild faces after injury or surgery

NCT ID NCT07654647

Disease control Sponsor: Tishreen University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tests whether custom 3D-printed titanium implants can safely and effectively rebuild facial bones in 30 adults with defects from injury, cancer surgery, or birth conditions. Each implant is designed from CT scans to match the patient's unique anatomy. Researchers will track complications, accuracy, and cosmetic results over time.

What this could mean

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

Active substance
Patient-specific 3D-printed titanium facial implants
What this could lead to
If successful, this could offer a reliable, custom-fit option for rebuilding facial bones and improving appearance after trauma, cancer surgery, or congenital defects.
What could go wrong
This is a small early study with only 30 people, so results may not apply to everyone. Risks include infection, implant failure, or the need for more surgery.

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

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

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2026

Expected to finish

Nov 2026

An estimate. End dates often move.

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.

Ages

18 to 60 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: * Age 18 years or older. * Presence of facial bone defects resulting from cystic or tumoral osteolytic lesions. * Acquired or congenital facial deformities associated with bony defects or facial asymmetry. * Patients requiring patient-specific 3D-printed titanium implants for maxillofacial reconstruction. * Aesthetic indications requiring custom facial implant design, including microgenia (chin retrusion). * Ability to provide written informed consent. Exclusion Criteria: * Active pathological lesions at the time of enrollment. * Age below 18 years. * History of radiotherapy within 12 months prior to enrollment. * Chronic untreated vitamin D deficiency. * Uncontrolled diabetes mellitus. * Inability or unwillingness to comply with follow-up requirements.

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Conditions

The condition(s) this trial relates to.

craniofacial microsomia Facial Asymmetry fibrous dysplasia hemifacial hypertrophy oral cavity squamous cell carcinoma Squamous Cell Carcinoma of Head and Neck Zygomycosis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Facial asymmetry Fibrous dysplasia Hemifacial microsomia Microgenia Mucormycosis Oral squamous cell carcinoma

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Ahmad Fayez Ahmad

    RECRUITING

    Latakia, Syria

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