Assessment of Dental Implants Placed in Posterior Maxillary Ridge Using Densah Burs Versus Standard Drills

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-09-01

Study Completion Date

2019-07-01

Brief Summary

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comparing the drilling technique of using densah burs osseo densification drills in posterior maxilla with the normal surgical kit drilling

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Detailed Description

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the densification of bone using the densah burs are thought to be improving the bone quality surrounding the implants thus increasing the primary stability and decreasing the marginal bone loss surrounding the implants comparing to the normal drilling techniques using the conventional implant drilling kit

Conditions

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Implant Site Reaction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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densah burs drilling group

implant osteotomy site drilling using the densah burs osseo densification drills

Group Type EXPERIMENTAL

densah burs osseo densification drills

Intervention Type DEVICE

osseo densification of the alveolar bone in maxillary posterior ridge during implant placement

surgical burs drilling group

implant osteotomy site drilling using conventional surgical burs drilling

Group Type ACTIVE_COMPARATOR

conventional surgical burs drilling

Intervention Type DEVICE

conventional implant osteotomy site drilling with implant surgical kit

Interventions

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densah burs osseo densification drills

osseo densification of the alveolar bone in maxillary posterior ridge during implant placement

Intervention Type DEVICE

conventional surgical burs drilling

conventional implant osteotomy site drilling with implant surgical kit

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients with partially edentulous in the posterior area of the maxilla, with a residual ridge that allowed insertion of ≤3.5 width implants.
* Both sexes.
* No intraoral soft and hard tissue pathology
* No systemic condition that contraindicate implant placement

Exclusion Criteria

* Sinus pathology.
* Heavy smokers more than 20 cigarettes per day.
* Patients with systemic disease that may affect normal healing.
* Psychiatric problems
* Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site
* Immunodeficiency pathology, bruxism, stress situation (socially or professionally), emotional instability, and unrealistic aesthetic demands.

Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes