Skip to content

Horizontal Ridge Augmentation Using Sausage Technique: A Retrospective Study

Horizontal Ridge Augmentation Using Sausage Technique: A Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07041398
Enrollment
23
Registered
2025-06-27
Start date
2024-01-02
Completion date
2024-06-10
Last updated
2025-06-27

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

Conditions

Alveolar Bone Grafting, Bone Gain, Guided Bone Regeneration

Keywords

Alveolar bone augmentation, Dental implant, Guided bone regeneration, Horizontal bone gain, Sausage technique

Brief summary

This retrospective study investigates the outcomes of the sausage technique, a contemporary modification of guided bone regeneration (GBR), for the augmentation of severely horizontally deficient alveolar ridges (\<4 mm width). The technique, originally introduced by Urban and colleagues, uses multiple fixation pins to enhance membrane stability and maintain graft volume through a tension dome effect. In this study, a total of 23 patients underwent horizontal ridge augmentation using the sausage technique, with bone measurements assessed at 2, 4, and 6 mm apical to the crest using CBCT imaging at preoperative (T0), early postoperative (T1), and late postoperative (T2) stages. The study quantitatively analyzed both horizontal bone gain (T2-T0) and bone resorption (T1-T2) during the healing period.

Interventions

None listed

Sponsors

Kocaeli University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with knife-edge alveolar ridges, classified as Class IV according to the Cawood and Howell classification, who underwent ridge augmentation using the sausage technique * Patients aged 18 or older with fully developed bone * Patients who had regular clinical and radiographic follow-up after the procedure, with a minimum follow-up period of six months

Exclusion criteria

* Patients with systemic conditions (such as osteoporosis, cancer, immunosuppression, hyperparathyroidism, or hyperthyroidism) or a history of medications (including intravenous or oral bisphosphonates, immunosuppressants, or chemotherapy) that could interfere with bone healing * Patients with a history of radiotherapy to the head or neck region * Patients classified as ASA III or ASA IV * Patients who were active smokers at the time of surgery * Patients whose pre- or postoperative CBCT scans were of low image quality or affected by artefacts

Design outcomes

Primary

MeasureTime frame
Amount of horizontal bone gain postoperativelyWithin1 week after the collection of patient data
Amount of horizontal bone resorption postoperativelyWithin 5 to 7 months postoperatively
Amount of vertical bone resorption postoperativelyWithin 5 to 7 months postoperatively

Countries

Turkey (Türkiye)

Outcome results

None listed

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