Assessment of Marginal Bone Loss and Anterior Implant Stability in Immediate Versus Early Implant Placement

NCT ID: NCT06985511

Last Updated: 2025-05-22

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

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-10

Study Completion Date

2024-02-15

Brief Summary

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This study aims to determine the differences in implant stability and measurement of bone loss near implants between two different healing approaches used for teeth replacement in the front part of the upper jaw.

Detailed Description

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Conditions

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Marginal Bone Loss

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

split-mouth design
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Immediate implant placement

Group Type EXPERIMENTAL

Immediate implant placement

Intervention Type PROCEDURE

Tooth extraction was performed atraumatically on one side, followed by immediate implant placement, right after extraction.

Early implant placement

Group Type ACTIVE_COMPARATOR

Early implant placement

Intervention Type PROCEDURE

The tooth was extracted, and the implant was placed four weeks later (early placement).

Interventions

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Immediate implant placement

Tooth extraction was performed atraumatically on one side, followed by immediate implant placement, right after extraction.

Intervention Type PROCEDURE

Early implant placement

The tooth was extracted, and the implant was placed four weeks later (early placement).

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Presence of unrestorable bilateral anterior teeth.
* Harmonious gingival contour and thick gingival phenotype
* Minimum 4 mm of apical bone and 2 mm of intact labial plate
* Absence of periapical pathology

Exclusion Criteria

* Systemic conditions affecting osseointegration or healing
* Active oral infections or periodontal disease
* Dehiscence or fenestration defects
* Poor oral hygiene or heavy smoking
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Yasser Ahmed

OTHER

Sponsor Role lead

Responsible Party

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Yasser Ahmed

Associate Professor of Prosthodontics

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Beirut Arab University

Beirut, , Lebanon

Site Status

Countries

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Lebanon

Other Identifiers

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IRB2023-H0113D-P-0494

Identifier Type: -

Identifier Source: org_study_id

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