Khoury's Bone Shell Technique Versus Titanium-Reinforced Polytetrafluoroethylene for Augmentation of Horizontal Deficiency in Posterior Mandible (Histomorphometry Analysis): A Randomized Clinical Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorBritish University In Egypt

About this trial

The purpose of the study is the comparison of bone gained histologically from the Bone Shell Khoury's Technique in comparison with the usage of non-resorbable membrane polytetrafluoroethylene and discussing its eligibility for implant placement in restoring the atrophic posterior mandible.

Eligibility criteria

Qualifiers

Have two or more missing teeth in the posterior mandibular segment.

The patients age of 18 and above.

The alveolar ridge in the edentulous site of the selected patients will have a buccolingual width of less than 4mm.

Sufficient vertical bone height.

Disqualifiers

Patients taking any medication that may interfere with bone healing or bone biology.

Patients with any systemic disease that may affect bone healing.

Any patients with any previous bone grafting procedure at the site of interest.

Smokers.

Trial design

Treatments tested in this trial

  • GBR using Ti based PTFE
  • Bone Shell Khoury's Technique

Treatment groups

16 Participants
are divided into 2 treatment groups

Sponsors and collaborators