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

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06653868
Enrollment
20
Registered
2024-10-22
Start date
2024-10-20
Completion date
2026-03-20
Last updated
2024-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Loss, Alveolar

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.

Interventions

PROCEDUREdental implant with bone augmentation

gap distance augmentation with bone graft

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
bone changes6 monthssuperimposition

Secondary

MeasureTime frameDescription
pink esthetic score6 monthssoft tissue esthetics

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026