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Comparison Between Different Horizontal Ridge Augmentation Techniques

Horizontal Ridge Augmentation Using Decompression Technique Versus Ridge Splitting in Atrophic Posterior Mandibular Ridge With Simultaneous Implant Placement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06176417
Enrollment
16
Registered
2023-12-19
Start date
2021-08-26
Completion date
2023-08-26
Last updated
2023-12-19

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

Conditions

Atrophic Ridge

Brief summary

Sixteen patients were selected from the Outpatient Clinic of the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University for replacement of missed single tooth / teeth in posterior atrophic mandible by dental implant. Patients' grouping: Patients were divided randomly into two equal uniform groups as follow: Group I: Eight implants were placed in patients of missing single tooth / teeth in posterior mandible with subsequent horizontal ridge augmentation by decompression technique. Group II: Eight implants were placed in patients of missing single tooth / teeth in posterior mandible with subsequent horizontal ridge augmentation by ridge splitting technique using piezosurgery. All patients were evaluated clinically and radiographically at regular time interval immediately, 6 and 12 months after surgery.

Interventions

PROCEDUREhorizontal ridge augmentation by decompression technique.

Instead of a cover screw, a 2-mm healing abutment was used after implant insertion

PROCEDUREhorizontal ridge augmentation by ridge splitting technique using piezosurgery.

horizontal ridge augmentation was done using piezosurgery tips and bone expanders

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Patient's cooperation, motivation and good oral hygiene. * Patient medically free from systemic diseases that absolutely contraindicate implant surgery. * Moderately atrophic posterior mandible (horizontal alveolar dimension is not more than 4 mm at the crest), with minimum 10 mm vertical height. * Patients prepared to comply with the follow-up and maintenance programme. * Free from history of bruxism / parafunctional habits.

Exclusion criteria

* Patients with local pathological disease such as cyst, tumor at the planned surgical site. * Pregnant patients. * Heavy smoker patients.

Design outcomes

Primary

MeasureTime frameDescription
Alveolar ridge width12 monthsThe ridge width was measured on the cross section view at different time interval from the outer surface of the buccal bone to the outer surface of the lingual bone perpendicular to the line marking the long axis of the implant at implant platform. Changes in alveolar ridge width was measured by subtracting ridge width value after 6 and 12 months from immediate postoperative.

Countries

Egypt

Outcome results

None listed

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