A Modified Sinus Floor Elevation Technique - a Pilot Study on 12 Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: sinus floor elevation.
- Who it may be relevant to
- Registry conditions: Maxillary Sinus, Atrophy. Basic parameters: 18 years — 100 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Austria
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
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.
Interventions
- Procedure sinus floor elevation
Primary outcome measures
- Height of augmentation [Time frame: after 4-5months]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Austria · 1 center
- Bernhard Gottlieb School of Dentistry, Medical University of Vienna — Vienna
Identifiers
NCT: NCT02137824 · 1