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Enrolling by invitation NCT07604155

Maxillary Sinus Augmentation Using CAD/CAM Allogenic Bone Blocks Versus Particulate Allogenic Grafts

No phase Interventional Maxillary Sinus Allograft

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: sinus lifting using CAD/CAM allogenic block, sinus lifting using particulate allogenic graft.
Who it may be relevant to
Registry conditions: Maxillary Sinus, Allograft. Basic parameters: from 20 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Maxillary Sinus Augmentation Using CAD/CAM Customized Allogenic Bone Blocks Versus Particulate Allogenic Grafts for Delayed Implant Placement: A Randomized Clinical Trial

Overview

28 patients will be included in this study with atrophic posterior maxillary ridge due to sinus pneumatization who will randomly assigned to two groups * Group I: sinus lifting using CAD/CAM allogenic block through lateral window technique * Group II: sinus lifting using particulate allogenic graftthrough lateral window technique

Detailed description

28patients will be included in this study with an atrophic posterior maxillary ridge due to sinus pneumatization, who will be randomly assigned to two groups

* Group I: sinus lifting using CAD/CAM allogenic block through lateral window technique * Group II: sinus lifting using particulate allogenic graft through the lateral window technique * Surgical procedure: A full-thickness, wide mucoperiosteal flap was elevated buccally. Alateral bony window of the maxillary sinus will be made then the sinus lining will be elevated carefully. The CAD/CAM allogenic block will be inserted and fixed in its position via a titanium screw to the crest of maxillary ridge (group I). In group II the particulate bone will be packed at the site of augmentation * The lateral window will be covered with collagen membrane, the flap will reposited in its place and sutured.

6 months later, implants will be inserted

Interventions

  • Procedure sinus lifting using CAD/CAM allogenic block
    A full-thickness, wide mucoperiosteal flap was elevated buccally. A lateral bony window of the maxillary sinus will be made, then the sinus lining will be carefully elevated. The CAD/CAM allogenic block will be inserted and fixed in its position via a titanium screw to the crest of maxillary ridge (group I). • The lateral window will be covered with collagen membrane, the flap will be repositioned in its place and sutured.
  • Procedure sinus lifting using particulate allogenic graft
    In group II the particulate bone will packed at the site of augmentation

Primary outcome measures

  • bone height gain [Time frame: 6 months]
  • marginal bone resorption around implants [Time frame: 6 months]

Eligibility criteria

Inclusion criteria

  • above 20 years
  • ridge height less than or equal to 5 mm
  • healthy clear sinus

Exclusion criteria

  • systemic disease affect bone healing
  • heavy smokers
  • disease or pathology within the sinus

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Faculty of Dentistry, Tanta University — Tanta

Identifiers

NCT: NCT07604155 · abcd

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗