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Clinical Trials/NCT06285903
NCT06285903
Completed
Not Applicable

Comparing the Hydrodynamic Piezoelectric Technique With Osseodensification for the Assessment of Internal Sinus Iift-ing: (a Randomized Clinical Trial)

Al-Azhar University1 site in 1 country20 target enrollmentSeptember 2, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bone Density, Low
Sponsor
Al-Azhar University
Enrollment
20
Locations
1
Primary Endpoint
Implant stability using the Osstell device by percentage
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Successful osseointegration considered the cornerstone in implant stability which predict the highest implants success outcomes. Implant stability depend on many factors like the implant design, surgical technique, and bone density. Posterior maxilla considered as a challenging area in implant placement, this is due to less dense trabecular bone sur-rounded by a thin layer of cortical bone which result in suffering in implant stability. The aim of this study is to evaluate the bone density outcomes using bone densification technique and piezoelectric surgical technique in sinus lift to promote bone gain

Detailed Description

Objectives: This study was directed to compare the outcomes of internal sinus lifting between osseodensification approach and piezoelectric surgery approach on the primary stability and osseointegration of dental implant. Background data: Successful osseointegration considered the cornerstone in implant sta-bility which predict the highest implants success outcomes. Implant stability depend on many factors like the implant design, surgical technique, and bone density. Posterior maxilla considered as a challenging area in implant placement, this is due to less dense trabecular bone surrounded by a thin layer of cortical bone which result in suffering in implant stability. The aim of this study is to evaluate the bone density outcomes using bone densification technique and piezoelectric surgical technique in sinus lift to promote bone gain. Materials and Methods: A total of 20 patients were randomly divided into two groups: Group1: patients received dental implant using osseodensification via Densah bur, Group2: patients received dental implant using hydrodynamic piezoelectric sinus lifting. The patients in both groups underwent bone grafting under sinus membrane. Modified bleeding index and probing depth were evaluated at 3, 6 and 12months intervals. An Osstell device was used to determine implant stability by recording the values of implant stability quotient (ISQ) immediately after implant placement and after 3 months. CBCT was performed before, after 6 months and after 12 months to evaluate ridge height, bone density. Marginal bone loss was evaluated after 3 months via periapical radiograph, after 6 , 12 months via CBCT.

Registry
clinicaltrials.gov
Start Date
September 2, 2022
End Date
December 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shaymaa Hussein Rafat Kotb

Assistant lecturere of oral medicine ,periodontology departement at sphinx university

Al-Azhar University

Eligibility Criteria

Inclusion Criteria

  • free of systemic disease bone height at the site of the implant is ≤ 6 mm. have good oral hygiene.

Exclusion Criteria

  • systemic diseases active periodontal disease , limited mouth-opening ability maxillary sinus disease or previous sinus surgery were also excluded smokers pregnant

Outcomes

Primary Outcomes

Implant stability using the Osstell device by percentage

Time Frame: baseline ,3 months

Primary implant stability (ISQ)

Secondary Outcomes

  • Modified sulcus bleeding index,Peri-implant pocket depth (PPD)by mm(3,6,9 months)

Study Sites (1)

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