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Clinical Trials/NCT03598049
NCT03598049
Unknown
Not Applicable

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

Cairo University0 sites30 target enrollmentSeptember 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Implant Site Reaction
Sponsor
Cairo University
Enrollment
30
Primary Endpoint
implant stability
Last Updated
7 years ago

Overview

Brief Summary

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

Detailed Description

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

Registry
clinicaltrials.gov
Start Date
September 1, 2018
End Date
July 1, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amira khaled ahmed

Principal Investigator

Cairo University

Eligibility Criteria

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.

Outcomes

Primary Outcomes

implant stability

Time Frame: at the time of surgery

measurement of implant stability using the ostell

Secondary Outcomes

  • Marginal bone loss(3 month)

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