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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05362136
Other study ID # 1709/2016
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 23, 2017
Est. completion date December 2027

Study information

Verified date May 2022
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the present study is to compare the rate of new bone formation after sinus floor elevation with or without perforation of the cortical sinus floor prior to insertion of augmentation material. Twelve patients requiring bilateral sinus floor elevation will be recruited for a pilot study in split-mouth design. On both sides a lateral window will be prepared and the sinus mucosa will be elevated. After this step, the sides are assigned as test or control side. While the control side is just filled with augmentation material, an additional step is performed for the test side, i.e., prior to inserting the augmentation material, the cortical bone layer of the sinus floor is perforated several times into the trabecular bone layer to improve the blood supply to the grafting material. Thereafter, both sides are left to healing for 4-6 months until implant installation. At timepoint of implant installation, a bone biopsy will be collected to allow histological assessment of the grafted area.


Recruitment information / eligibility

Status Recruiting
Enrollment 12
Est. completion date December 2027
Est. primary completion date December 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 120 Years
Eligibility Inclusion Criteria: - in need of bilateral sinus floor elevation - residual alveolar ridge height 2-6mm - residual alveolar ridge width > 4mm Exclusion Criteria: - uncontrolled periodontal disease - acute or chronic sinusitis

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
perforation of the sinus floor
perforation of the cortical layer of the sinus floor prior to inserting the augmentation material during sinus floor elevation
no perforation of the sinus floor
standard procedure for sinus floor elevation

Locations

Country Name City State
Austria University Clinic 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 New bone formation histological assessment of new bone formation after sinus floor elevation (%) 4-6 months after sinus floor elevation
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