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Efficacy of Mixture of Vancomycin With Xenograft for Immediate Implant Placement in Chronic Infected Socket

Efficacy of Mixture of Vancomycin With Xenograft for Immediate Implant Placement in Chronic Infected Socket (Clinical and Radiographic Study)

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07784075
Acronym
RCT
Enrollment
20
Registered
2026-08-25
Start date
2024-07-10
Completion date
2025-04-01
Last updated
2026-08-25

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

Conditions

Immediate Implant Placement in Chronic Infected Socket

Keywords

Immediate dental implant, Infected Socket, Bone preservation,, Xenograft,, Vancomycin., Local delivery antibiotic

Brief summary

Adding local vancomycin to xenografts greatly benefits stability, bone density, and limits marginal bone loss in dental implants in infected socket.

Detailed description

Aim: to evaluate how adding vancomycin to the xenograft in the infected socket affects bone preservation during immediate implant placement. Background: Proper dental implant placement is crucial for successful osseointegration, as the resultant tiny gaps between the implant and bone can affect implant stability. These gaps are better filled with xenografts, which are easy to handle, widely available, and provide an osteoconductive framework that supports better implant outcomes. It's also important to prevent nearby infections, since the infected socket can damage both soft and hard tissues, raising the risk of peri-implantitis and further implant failure. Applying locally delivered antibiotics during placement can help protect and manage against early infections. Patients and methods: Twenty patients with mandibular extraction sockets participated in the study divided into two groups: 10 patients received a xenograft mixed with vancomycin (Group I), and 10 patients received a xenograft alone (Group II). Implant stability was assessed clinically at baseline and at 6 months only, while CBCT scans were used to monitor crestal bone loss and bone density at baseline, 6 months, and 9 months. Post-surgical complications were also monitored throughout the study period.

Interventions

PROCEDUREimmediate dental implants Placement in Chronic Infected Socket

(Clinical and Radiographic Study)

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Clinical and Radiographic Study

Eligibility

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

Inclusion criteria

* a badly decayed, hopeless tooth with periapical infection indicated for extraction and seeking implant placement

Exclusion criteria

* Acute infected socket. * Any socket with more than four wall defects.

Design outcomes

Primary

MeasureTime frameDescription
implant stabilitybaseline, 1, 6 months after implant placementChanges in ISQ utilizing the Ostell ™ system

Secondary

MeasureTime frameDescription
bone marginal levelbaseline, 1, 6 and 9 months after treatmentRadiographic evaluation: Marginal bone height at the mesial and distal surfaces was measured in the panoramic view of the CBCT software, while the buccal and palatal surfaces were assessed in the cross-sectional view.
measure bone densitybaseline, 1, 6 and 9 months after treatmentRadiographic evaluation,using CBCT software, the average density of the marginal and crestal bone around the implant was measured

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 26, 2026