Diode Laser Photocoagulation With Immediate Implant Placement

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

8 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-30

Study Completion Date

2026-02-25

Brief Summary

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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.

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Detailed Description

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Conditions

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Tooth Extraction Immediate Dental Implant Photocoagulation Maxillary Esthetic Zone

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Immediate implant with photocoagulation

Group Type EXPERIMENTAL

Diode laser and Immediate implant

Intervention Type OTHER

patients with non-restorable teeth in the maxillary esthetic zone will be included in this prospective single-arm study. The non-restorable tooth will be atraumatically extracted and immediate implant placement will be placed. The extraction socket will be sealed with diode laser photocoagulation and customized healing abutments fabrication.

Interventions

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Diode laser and Immediate implant

patients with non-restorable teeth in the maxillary esthetic zone will be included in this prospective single-arm study. The non-restorable tooth will be atraumatically extracted and immediate implant placement will be placed. The extraction socket will be sealed with diode laser photocoagulation and customized healing abutments fabrication.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with non-restorable maxillary teeth in the aesthetic zone are indicated for extraction and subsequent immediate implant placement, including those with:
* 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.
* Patients with an extraction socket Type I.
* A good standard of oral hygiene.

Exclusion Criteria

* 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.
* Heavy smokers.
* Systemic conditions
* History of oral or intravenous bisphosphonate therapy or any treatments with other medications that may interfere with bone metabolism within the past 12 months

Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No