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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02137824
Other study ID # 1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date December 2030

Study information

Verified date March 2023
Source Medical University of Vienna
Contact Kristina Bertl, PD, DMD, MSc
Email kristina.bertl@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date December 2030
Est. primary completion date December 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
sinus floor elevation


Locations

Country Name City State
Austria Bernhard Gottlieb School of Dentistry, Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Height of augmentation after 4-5months
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