Three-Dimensional Bone Augmentation of Severely Atrophied Posterior Mandibular Alveolar Ridges Using Customized-3D Zirconia Barriers Versus Pre-bent Titanium Mesh

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-50
SponsorHams Hamed Abdelrahman

About this trial

Zirconia can be considered as an alternative and innovative material suitable for GBR because it has high biocompatibility, together with a scarce tissue integration. Zirconia barriers could be a predictable and alternative barrier material for GBR in terms of (i) biocompatibility, (ii) ease of use and removal, (iii) exposure management, (iv) bone regeneration outcomes.

Eligibility criteria

Qualifiers

Patients are systemically medically free according to the American Society of Anesthesiologists (ASA) considered as ASA I.

Ability to maintain good oral hygiene as evidenced in recall visits.

patients who had a partial or completely edentulous alveolar ridge with apparent 3D defect following teeth loss.

All patients were free from any local or general disease that may interfere with bone healing and had no history of previous grafting procedure at the designated edentulous ridge.

Disqualifiers

Smoker (> 25 cigarettes/ day).

Patients undergoing radiotherapy or chemotherapy

Patients having infection or local lesions in the area of surgery.

Patients with diabetes mellitus or bone diseases which may compromise the results.

Trial design

Treatments tested in this trial

  • customized Zirconia barrier
  • prebent titanium mesh

Treatment groups

16 Participants
are divided into 2 treatment groups

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Kafr El-sheikh UniversityRecruiting Kafr ElsheikhEgyptEgypt

Sponsors and collaborators

Hams Hamed Abdelrahman

Lead sponsor

Alexandria University

Sponsor institution