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Grafting of the Peri-implant Bony Defects Around Immediate Implants Using Xenogenic Versus Alloplastic Sticky Grafts: Randomized Controlled Clinical Trial

Not Applicable
Recruiting
Conditions
Bone Loss, Alveolar
Registration Number
NCT06653868
Lead Sponsor
Cairo University
Brief Summary

In patients with a single non restorable tooth, does filling the peri-implant buccal gap with alloplastic sticky grafts result comparable results compared to xenogenic sticky grafts?

Detailed Description

The buccal aspect of the dental implant has great importance, especially in the aesthetic zone, because the buccal bone is very thin especially in the anterior maxilla and its resorption can result in recession of the soft tissue. A gap occurs in immediately placed implant due to discrepancy between the dimensions of the extraction socket and the implant. Augmentation of the buccal gap decreases the amount of buccal bone resorption and soft tissue recession . Filling the peri-implant defects has been widely discussed to prevent further bone loss. The use of biologic materials such as platelet rich fibrin can enhance the quality of alloplastic bone grafts to give comparable effect when compared to xenogenic grafts.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  1. Patients with healthy systemic condition (Mazzotti et al., 2023).

  2. Age from 20-50 years old

  3. Patients must be free of any systemic disease which could influence the surgical procedure.

  4. Tooth involved in the esthetic zone.

  5. Sufficient hard and soft tissue volume in vertical and buccolingual direction

  6. Natural teeth adjacent to the involved tooth will be required to be free from infection.

  7. Controlled oral hygiene.

  8. Indication for tooth extraction included (Degidi et al., 2012);

    • Endodontic failures
    • Untreatable caries
    • Non- restorable teeth
    • Vertical root fracture
    • Remaining roots
Exclusion Criteria
  • 1.Pregnant females 2.Smokers (Khuller, 2009) 3.Unmotivated and uncooperative patients with poor oral hygiene 4.Patients with habits that may compromise the longevity and affect the result of the study as alcoholism or parafunctional habits.

5.Presence of acute dento-alveolar infection.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
bone changes6 months

superimposition

Secondary Outcome Measures
NameTimeMethod
pink esthetic score6 months

soft tissue esthetics

Trial Locations

Locations (1)

Cairo University

🇪🇬

Cairo, Egypt

Cairo University
🇪🇬Cairo, Egypt
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