Comparison of Two Pre-prosthetic Surgical Techniques for Augmentation of Mandibular Vertical Ridge Defects

  • STATUS
    Recruiting
  • participants needed
    14
  • sponsor
    Lydia Nabil
Updated on 19 February 2024

Summary

The aim of this study is to compare two pre-prosthetic surgical techniques for augmentation of vertical mandibular ridge defects in preparation for implant placement, the first using customized ceramic membranes and the second using tenting titanium screws in conjunction with particulate bone graft and collagen membrane (modified sausage technique).

Description

Background: Expansion of the periosteum and soft tissue matrix by tenting has been described as a method of Guided Bone Regeneration (GBR) for reconstruction of atrophic alveolar ridges.

Materials and Methods: The current study is a prospective controlled clinical trial, conducted on 14 patients, having about 7 mm of vertical bone height in the posterior mandible above the inferior alveolar canal. They are divided into 2 equal groups, each consisting of 7 patients. The first group receives customized ceramic membranes with a vertical height 5 mm above the crest of the ridge to tent out the soft tissue matrix, while in the second group, tenting of the soft tissue is done by fixation of two tenting screws, particulate bone graft is packed then covered by collagen membrane that is fixed by bone tacks (modified sausage technique).

Details
Condition Alveolar Ridge Enlargement
Age 40-60 years
Treatment customised ceramic sheets (Group 1), modified sausage technique (Group 2)
Clinical Study IdentifierNCT04376320
SponsorLydia Nabil
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

patients of both genders
with age range from 40 to 60 years
having about 7 mm of vertical bone height in the posterior mandible above the inferior alveolar canal and
requiring prosthetic rehabilitation with dental implants

Exclusion Criteria

heavy smokers
patients undergoing radiotherapy or chemotherapy
those having infection or local lesions in the area of surgery, and
patients with bone diseases which may compromise the results
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