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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02137824
Enrollment
12
Registered
2014-05-14
Start date
2014-05-31
Completion date
2030-12-31
Last updated
2023-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrophy, Maxillary Sinus

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.

Interventions

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
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

Design outcomes

Primary

MeasureTime frame
Height of augmentationafter 4-5months

Countries

Austria

Contacts

Primary ContactKristina Bertl, PD, DMD, MSc
kristina.bertl@meduniwien.ac.at

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026