Reconstruction Implant Bone After Removal Using Porous Titanium Prosthesis

Status Completed

Clinical Trial Summary

This trial will study the reconstruction of the anterior part of the mandible and the adjacent soft tissue parts by a mandibular prosthesis made in porous titanium, associated or not, to a latissimus dorsi or pectoral flap, to avoid reconstruction with free microanastomosed bone flaps that are often associated with important morbidity.

The implant is consolidated by two prolonged parallel plates of titanium, allowing their fixation to the bone, easy to fix in a short time.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Otorhinolaryngologic Diseases

Clinical Trial Details

NCT number	NCT00213837
Study type	Interventional
Source	University Hospital, Strasbourg, France
Contact
Status	Completed
Phase	Phase 2
Start date	October 2003
Completion date	September 2008

View Details

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