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
| Type | Name | Description |
|---|---|---|
| DEVICE | Poly 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.