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Modified Surgical Technique for Lateral Block Augmentation Prior to Implant Installation

Medical University of Vienna logo

Medical University of Vienna

Status

Active, not recruiting

Conditions

Bone Augmentation

Treatments

Other: block perforation

Study type

Interventional

Funder types

Other

Identifiers

NCT05339971
1401/2016

Details and patient eligibility

About

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.

Enrollment

10 patients

Sex

All

Ages

18 to 130 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

block perforation
Experimental group
Treatment:
Other: block perforation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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