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Clinical Trials in Egypt / NCT07705399
Active, not recruiting Not applicable

Evaluation of Autogenous Bone Graft on Immediate Dental Implant Osseointegration Using Piezosurgery

NCT07705399 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-05-17
Last updated
2026-07-15

Condition(s) studied

Tooth LossPartial Edentulism in the Maxilla or in the Mandible

Investigational drug(s) / intervention(s)

Immediate implant with autogenous bone graftImmediate implant without bone graft

Immediate implant with autogenous bone graft: Immediate implant with autogenous bone graft using piezo surgery

Immediate implant without bone graft: Immediate implant without bone graft

Study summary

This clinical study aims to evaluate the clinical and radiographic outcomes of immediate dental implant placement in mandibular premolar sites. Patients requiring extraction of mandibular premolars will receive immediate implant placement, with or without autogenous bone grafting, according to the study protocol.

When indicated, autogenous bone graft will be harvested using piezosurgery during the implant procedure. Participants will be followed up clinically and radiographically to assess implant stability, marginal bone level changes, and peri-implant tissue conditions over a defined follow-up period. The results of this study may help determine the effectiveness and predictability of immediate implant placement in mandibular premolar regions.

Eligibility

Sex
ALL
Min age
25 Years
Max age
45 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Patients requiring extraction of mandibular premolars. * Age ≥ 25 years. * Adequate oral hygiene and motivated patients for implant treatment. * Sufficient bone volume to allow immediate implant placement (with or without minor augmentation). * Patients willing to participate and attend follow-up visits for at least 6 months. * Systemically healthy patients (ASA I or II). Exclusion Criteria: * Uncontrolled systemic diseases (e.g., uncontrolled diabetes, immunocompromised patients). * Heavy smokers (e.g., \>10-15 cigarettes/day). * Active periodontal or acute infection at the implant site. * Poor oral hygiene or non-compliant patients. * Pregnancy or lactation. * History of radiotherapy in head and neck region. * Severe bone deficiency not suitable for immediate implant placement.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Suez Canal University, Faculty of Dentistry Ismailia Egypt

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07705399 on ClinicalTrials.gov ↗ ← All trials in Egypt