About this trial
Placement of an immediate implant is becoming popular because of its potential in minimizing the treatment time and enhancing the patient comfort and esthetic outcomes. It is crucial to maintain adequate thickness of labial bone with the establishment of a stable and healthy gingival seal around the implant abutment to prevent the invasion of bacteria and peri-implant inflammation. Diode lasers have been developed as a promising tool in dentistry, providing a precise manipulation and photocoagulation effect that may have a positive influence on both bone remodeling and soft tissue healing. This study aims to evaluate the effectiveness of the utilization of diode laser photocoagulation with immediate implant placement and customized healing abutment in the maxillary esthetic zone.
Eligibility criteria
Qualifiers
A severely carious tooth that cannot be restored.
Pulpal necrosis or irreversible pulpitis that is not amenable to endodontics.
Periodontally involved teeth with grade 2 mobility or above.
Teeth with root caries that can't be restored.
Disqualifiers
Patients with extraction socket Type II or III, with buccal plate defects.
Absence of at least 2 mm of bone apical to the extraction socket
tooth ankylosis.
Patients with deciduous teeth.
Trial design
Treatments tested in this trial
- Diode laser and Immediate implant
Treatment groups
Sponsors and collaborators
Hams Hamed Abdelrahman
Lead sponsor
Alexandria University
Sponsor institution