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Orbital Fractures clinical trials

View clinical trials related to Orbital Fractures.

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NCT ID: NCT06369129 Recruiting - Orbital Fractures Clinical Trials

Accuracy& Orbital Volume Using Patient Specific Titanium Implant Vs Zirconia for Orbital Floor Reconstruction

Start date: April 6, 2024
Phase: N/A
Study type: Interventional

Comparative study used to assess if the patient specific zirconia implant will provide better accuracy, intraoperative adaptability, precise orbital volume and soft tissue reaction with more cost effectiveness than the patient specific titanium implants in orbital floor reconstruction after blow out fractures .

NCT ID: NCT06294535 Enrolling by invitation - Orbital Fractures Clinical Trials

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

Start date: December 11, 2023
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT05439512 Completed - Orbital Fractures Clinical Trials

Orbital Floor Fracture Repair by Titanium Mesh Via Transantral Approach.

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the feasibility of CAD/CAM osteosynthesis mesh through a transantral surgical approach in the Repair of orbital floor fractures by means of clinical and radiographic findings.

NCT ID: NCT05438784 Recruiting - Zygomatic Fractures Clinical Trials

Application of CAD-CAM Technology in Orbital Bone Reconstruction

CAD-CAM
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Reconstruction of orbital defects resulting after trauma; tumor resection; maxillary cyst; craniofacial anomalies and sequestrated boneā€¦. etc., has been a challenging issue over the years and this owing to the complicated anatomy of orbit. Inaccurate orbital reconstruction may lead to devastating cosmetic and functional complications. Titanium mesh for orbital reconstruction has now become "probably" the most popular material for orbital wall reconstruction worldwide. Innovation of CAD-CAM technology and its application in maxillofacial surgery will markedly improve the surgical outcome. This study will assess the accuracy of orbital reconstruction using CAD-CAM technology and to compare two different modalities for orbital reconstruction based on this technology.

NCT ID: NCT04704414 Recruiting - Clinical trials for Graves Ophthalmopathy

Exophthalmometry With 3D Face Scanners

EX3D
Start date: August 14, 2019
Phase: N/A
Study type: Interventional

This study investigates diagnostic methods to measure eyeball protrusion with a smartphone face scanner compared to the traditional Hertel exophthalmometer. The study aims to validate a new reliable, fast and convenient smartphone app to measure the protrusion of the eyeball in different diseases such as Graves' disease, orbital tumors, orbital fractures or orbital inflammation, as well as other rare diseases.

NCT ID: NCT04271137 Not yet recruiting - Orbital Fractures Clinical Trials

Correction of Enophthalmos and Orbital Volume Using Pre-bent Mesh Versus 3d Printed Onlay in Orbital Fracture Cases

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

this study evaluates the post-surgical correction of enophthalmos and orbital volume using 3D printed only versus pre-bent titanium mesh in blow-out fracture cases

NCT ID: NCT03887988 Recruiting - Orbital Fractures Clinical Trials

Orbital Fractures Registry

OFx
Start date: November 1, 2019
Phase:
Study type: Observational [Patient Registry]

Approximately 300 patients presenting orbital blow-out fracture will be enrolled prospectively in this registry. All patients, surgically and nonsurgically treated as per standard (routine) of care will be followed-up (FU) within the registry for a period of 6 months.

NCT ID: NCT03813732 Not yet recruiting - Orbital Fractures Clinical Trials

Using the Transconjuctival Approach Alone Versus Using it Together With Lateral Canthotomy in Orbital Fractures

Start date: January 15, 2019
Phase: N/A
Study type: Interventional

All cases will undergo surgery under general anesthesia. Evaluation of patients with suspected orbital fracture should involve radiologic examination, motility test, diplopia field test and exophthalmometry. Plain X-ray films, although rarely used, with the Caldwell and Waters view may be done as a screening evaluation for possible fractures and foreign bodies. An orbital computed tomography, the gold standard in trauma, CT with contiguous thin axial and coronal sections should be ordered to confirm the diagnosis and plan for treatment Postoperative care: Proper postoperative instructions will be given the patient, in addition to the postoperative medications including antibiotics, corticosteroids and analgesics.

NCT ID: NCT03673865 Terminated - Orbital Fractures Clinical Trials

The Use of 3D Printing in Orbital Fractures

Start date: October 11, 2019
Phase: N/A
Study type: Interventional

The study is a prospective randomized longitudinal clinical study to compare pre-adapted patient-specific orbital implants utilizing an office-based 3-D printer versus standard non-adapted orbital implants (the latter being the traditional approach and current standard of care).

NCT ID: NCT03057405 Completed - Orbital Fractures Clinical Trials

Intra-operative (IO) Navigation and IO-CBCT for 3D Orbital Reconstruction

Start date: October 2016
Phase:
Study type: Observational

Background Correction of post traumatic and post-ablative orbita defects remains a challenge for the maxillofacial surgeon. The purpose of such intervention is the restoration of both function and aesthetics by anatomical reconstruction of the bony orbitawalls, with attention to the orbitavolume. Unfortunately, the results of such interventions today are still somewhat unpredictable. The aim of this study is to determine whether 3D virtual planning combined with intra-operative navigation can increase the predictability of the outcome in function and aesthetics. Study design Retrospective study. Demographic data, diagnostic and surgical parameters will be collected of all patients undergoing orbital surgery between 01/01/2012 and 31/12/2016 at the department. Pre- en postoperative orbit volume will be determined based on CT-analysis in Brainlab software, and compared to the non-defected orbit.