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Clinical Trials/NCT02137824
NCT02137824RecruitingNot Applicable

A Modified Sinus Floor Elevation Technique - a Pilot Study on 12 Patients

Medical University of Vienna2 sites in 1 country12 target enrollmentStarted: May 2014Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
12
Locations
2
Primary Endpoint
Height of augmentation
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The aim of the present study is to establish a modified minimally invasive surgical technique for sinus floor augmentation with a residual bone height of 3-6mm.

Hypothesis: The investigators expect that the present surgical technique allows to achieve an adequate implant bed of at least 10mm height after a healing period of 3-5 months. Further the modification of the technique enables a reduced patient stress level.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •residual bone height of 3-6mm
  • •residual bone width of >4mm

Exclusion Criteria

  • •not treated periodontal disease
  • •smoker (>5cig/day)
  • •acute or chronic sinusitis

Outcomes

Primary Outcomes

Height of augmentation

Time Frame: after 4-5months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kristina Bertl

PD, DMD, MSc

Medical University of Vienna

Study Sites (2)

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