Maxillary Sinus Augmentation Via the "Bone Lid Technique"

NCT ID: NCT06222970

Last Updated: 2024-01-30

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

RECRUITING

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-05-04

Study Completion Date

2024-12-31

Brief Summary

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Maxillary sinus augmentation is one of the most performed procedures to increase the bone quantity of the atrophic maxilla in order to allow implant placement. The aim of the present case series was to describe a surgical protocol to perform maxillary sinus augmentation with the "bone lid technique", and its outcomes in a cohort of patients eligible for the procedure.

Detailed Description

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Conditions

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Maxillary Deficiency

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Bone lid repositioning in course of sinus lift

A full-thickness flap was elevated to access the lateral maxillary bone wall. Subsequently, a lateral access window was prepared using a piezoelectric device with specific bone tips, delimitating a trapezoidal bone lid.

Once the antrostomy was completed, the bone lid was gently removed with a Lucas surgical curette and anatomical tweezers, with great care to avoid damages to the Schneiderian membrane. The Schneiderian membrane was detached from the bone layer using specific sinus curettes. In case of sinus membrane perforation, the membrane was raised in all directions. All clinical cases received a cortical bone lamina to avoid graft particles displacement in the maxillary sinus. The elevated space was filled with chips of cortico-spongious bone. The antrostomy was then covered with the bone lid (osteotomy window), previously removed and preserved in physiological solution and fixed in the original anatomical position with a surgical glue. The flap was then repositioned and sutured.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Partially or fully edentulous patients requiring an implant-prosthetic rehabilitation of the premolar or molar maxillary areas with a residual ridge height lower than 4 mm.
* Patients needing for a unilateral or bilateral sinus lift with a lateral wall approach.

Exclusion Criteria

* Patients under treatment with immunosuppressive agents
* Patients under treatment with medications that could impair bone metabolism.
* Patients pregnant or breastfeeding.
* Patients who had received irradiation treatment to the head and neck area.
* Patients with uncontrolled diabetes.
* Patients with uncontrolled periodontal disease.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Pisa

OTHER

Sponsor Role lead

Responsible Party

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Antonio Barone

Full Professor of Oral Surgery and Implantology, Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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U.O. Odontostomatologia e Chirurgia del Cavo Orale

Pisa, , Italy

Site Status RECRUITING

Countries

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Italy

Facility Contacts

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Antonio Barone, Professor

Role: primary

050993327

Other Identifiers

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SINUSLID_2023

Identifier Type: -

Identifier Source: org_study_id

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