Clinical Trials Directory

Trials / Unknown

UnknownNCT03265795

Validity of PEEK PSI Containing Autogenous Bone Graft for Maxillary Reconstruction Following Lesion Enucleation

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
8 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
15 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Surgical ablation of large maxillary cysts usually results in considerable hard and soft tissue deficits that ultimately affect the final esthetic and functional outcomes. Reconstruction of such defects; whether primarily or secondarily; offers much better long-term outcomes. However, primary bony reconstruction becomes potentially complicated in many cases of such large cysts encroaching or involving the maxillary sinus where a communication with the maxillary sinus lining may be unavoidable. Reconstruction of such defects can be accomplished using either vascularized or; more commonly; non-vascularized autogenous bone grafts. Different bone substitutes remain to be another viable option. The simultaneous use of titanium meshes provides physical three-dimensional support for the bone graft contained within as well as the overlying soft tissues. However, the drawbacks of titanium meshes in such defects remain to be mainly the difficulty in adequately shaping the mesh and the lack of proper isolation of the mesh contents from the maxillary sinus cavity.

Conditions

Interventions

TypeNameDescription
DEVICEPoly Ether Ether Ketone PSI (patient specific implant).reconstruction of the bone and the original volume of maxillary sinus accurately (in terms of clinical and radiographic parameters).

Timeline

Start date
2018-01-01
Primary completion
2018-03-01
Completion
2018-07-01
First posted
2017-08-29
Last updated
2017-08-30

Source: ClinicalTrials.gov record NCT03265795. Inclusion in this directory is not an endorsement.