Clinical Trials Directory

Trials / Completed

CompletedNCT06294535

The Accuracy of Reconstruction of Orbital Walls Fracture Using Prebent Mesh Versus Patient Specific Implant

The Accuracy of Reconstruction of Orbital Walls Fracture Using Prebent Mesh Versus Patient Specific Implant : A Prospective Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Tanta University · Academic / Other
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

under GA, incision to access to orbital walls. Then insertion of prebent titanium mesh or customized titanium implant and fixation with miniscrews, examination of ocular motility using forced duction test followed by closure of flap.

Detailed description

under GA, incision to access to orbital walls. complete reflection of orbital floor to be constructed then insertion of customized orbital implant of patient or insertion of titanium mrsh after adaption on the model and fixation with miniscrews, examination of ocular motility using forced duction test followed by closure of flap.

Conditions

Interventions

TypeNameDescription
DEVICEreconstruction of orbital wallsunder GA, incision to access to orbital walls. Then insertion of prebent titanium mesh or customized titanium implant and fixation with miniscrews, examination of ocular motility using forced duction test followed by closure of flap.

Timeline

Start date
2023-12-11
Primary completion
2024-05-18
Completion
2024-12-06
First posted
2024-03-05
Last updated
2025-05-06

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06294535. Inclusion in this directory is not an endorsement.