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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05339971
Other study ID # 1401/2016
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 7, 2016
Est. completion date December 2024

Study information

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

Clinical Trial Summary

Evaluation of the surgical result (augmentation volume, proportion of newly formed bone) after perforation of the bone block in the course of lateral block augmentation prior to planned implant installation.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 10
Est. completion date December 2024
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 130 Years
Eligibility Inclusion Criteria: - single tooth gap in need of lateral bone augmentation prior to implant installation Exclusion Criteria: - untreated periodontal disease - systemic disease and/or medication intake with significant effect on bone healing

Study Design


Related Conditions & MeSH terms


Intervention

Other:
block perforation
The bone block used for lateral bone augmentation will be perforated several times.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Outcome

Type Measure Description Time frame Safety issue
Primary Histomorphometry % of new bone formation at implant installation (approximately 6 months after augmentation)
Primary Radiographic Volume gain (mm3) after block augmentation at the buccal aspect 6 months after block augmentation
Primary Radiographic Volume gain (mm3) after block augmentation at the buccal aspect 12 months after block augmentation
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