Can 3D-printed plastic implants keep eyes level after jaw tumor removal?
NCT ID NCT07789392
First seen Aug 27, 2026 · Last updated Sep 09, 2026 · Updated 2 times
Summary
This trial tests whether patient-specific PEEK implants, custom-made plastic pieces, can rebuild the bone under the eye after surgery to remove part of the upper jaw due to tumors. The goal is to keep the eye in its natural position and avoid a sunken appearance or vision problems. Nine people who need this type of jaw and eye socket reconstruction will receive the implant. Researchers will measure eye position and socket volume using CT scans, and watch for complications like double vision or eyelid issues.
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 PEEK implants, a custom-made plastic device used to rebuild the bone under the eye after tumor removal surgery
- What this could lead to
- If it works, this could give people who lose part of the upper jaw to tumors a reliable way to rebuild the eye socket, reducing sunken-eye appearance and vision problems after surgery.
- What could go wrong
- This is a small, early-stage trial with only 9 participants, so results may not apply to everyone. Surgery carries risks like infection, implant movement, or eye complications such as double vision or eyelid issues.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
6 people
The number who actually took part.
- Started
-
Oct 2023
- Finished
-
Feb 2026
- 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 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: 1\. Unilateral invasive benign or malignant tumors of the maxilla that requires orbital floor resection. 3\. Brown class III maxillectomy defects patients 2. Patients with immediate orbital floor reconstruction will be enrolled in this study. Exclusion Criteria: 1. Medically compromised patients contradicting operation. 2. Delayed orbital floor reconstruction cases will be excluded. 3. Bilateral cases will be excluded.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Maxillectomy are added.
By submitting, you agree to our Terms of use
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
-
Faculty of dentistry, Alexandria university
Alexandria, 21523, Egypt