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Clinical Trials/NCT03732885
NCT03732885UnknownNot Applicable

Crestal Maxillary Sinus Floor Elevation Using Osseodensification Drills (Densah Burs) Versus Summers Osteotomes

Cairo University1 site in 1 country24 target enrollmentStarted: November 1, 2018Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
24
Locations
1
Primary Endpoint
implant stability
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

To investigate the efficacy of osseodensification drills (Densah bure) as a new closed sinus lift tool and to compare the effect of it in bone gaine versus traditional osteotomes.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
25 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patients with partially edentulous in the posterior area of the maxilla, with a residual ridge that allowed insertion of ≤8 mm length 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.

Arms & Interventions

densah burs drilling group

Experimental

maxillary sinus floor elevation during implant placement using Densah burs

Intervention: densah burs osseo densification drills (Device)

Summers osteotomes

Experimental

maxillary sinus floor elevation during implant placement using Summer's Osteotomes

Intervention: Summer's Osteotomes (Device)

Outcomes

Primary Outcomes

implant stability

Time Frame: 6 months after surgery

measurement of implant stability using the Ostell

Secondary Outcomes

  • bone gain(6 months after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sohaib Mohamed Alzamzamy Mohamed Elsheikh

principal investigator

Cairo University

Study Sites (1)

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