Modified Surgical Technique for Lateral Block Augmentation Prior to Implant Installation

Modified Surgical Technique for Lateral Block Augmentation Prior to Implant Installation - A Pilot Study on 10 Patients With Histological Assessment

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05339971

Enrollment

Registered

2022-04-21

Start date

2016-12-07

Completion date

2024-12-31

Last updated

2022-04-21

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

Conditions

Bone Augmentation

Brief 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.

Interventions

OTHERblock perforation

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

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 130 Years

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

Design outcomes

Primary

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

Outcome results

None listed

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