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Clinical and Radiographic Evaluation of Delayed Dental Implant Placement After Socket Preservation Using Injectable Bone Graft

Clinical and Radiographic Evaluation of Delayed Implant Placement Following Socket Preservation With Injectable Alloplastic Bone Graft. A Randomized Controlled Study.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07373600
Enrollment
20
Registered
2026-01-28
Start date
2026-01-01
Completion date
2027-11-01
Last updated
2026-01-28

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

Conditions

Alveolar Ridge Preservation, Dental Implant Placement

Keywords

Dental Implant Placement, Alveolar Ridge Preservation

Brief summary

This clinical study aims to evaluate the clinical and radiographic outcomes of delayed dental implant placement following socket preservation using an injectable alloplastic bone graft material. The study will include patients who require tooth extraction and are candidates for implant placement. After tooth extraction, the socket will be preserved using the bone graft material, and dental implants will be placed after a healing period. Clinical and radiographic assessments will be performed to evaluate bone quality, bone height, and implant stability. The goal of this study is to determine the effectiveness of injectable alloplastic bone grafts in maintaining the alveolar ridge and improving the success of delayed implant placement.

Interventions

DEVICEInjectable Alloplastic Bone Graft

Following tooth extraction, socket preservation will be performed using an injectable alloplastic bone graft material composed of biocompatible synthetic components. The material will be placed into the extraction socket to maintain ridge dimensions and promote bone regeneration. After a healing period of several months, delayed implant placement will be performed, and clinical and radiographic evaluations will assess ridge preservation and implant success

Sponsors

Suez Canal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Patient aged between 40 and 60 years * General good health. * Volunteer subjects have to voluntarily sign an informed consent. * Patient Indicated for single implant placement in lower posterior area. Inclusion criteria for patients in group I · Patient with a previously extracted lower posterior tooth and the socket was preserved with injectable bone graft .

Exclusion criteria

* Patient with systemic disease affection bone metabolism . * Patients with contraindication to surgical treatment. * Patients with uncontrolled medical conditions.

Design outcomes

Primary

MeasureTime frameDescription
Implant stability at the time of delayed implant placementAt the time of delayed implant placement (approximately 4 to 6 months after tooth extraction)Implant stability will be assessed at the time of delayed implant placement using resonance frequency analysis (RFA) to obtain implant stability quotient (ISQ) values. The ISQ readings will be used to evaluate the effect of socket preservation with injectable alloplastic bone graft on implant stability in comparison to sites without grafting.

Outcome results

None listed

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