Skip to content

Horizontal Bone Augmentation - comparison of Dome Technique with Guided Bone Regeneration: randomized clinical study

Horizontal Bone Augmentation of the Alveolar Ridge using the Polydioxanone Dome Technique versus Guided Bone Regeneration: a randomized clinical trial -

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
REBEC
Registry ID
RBR-2x5w7rf
Enrollment
Unknown
Registered
2025-09-25
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Jaw, Edentulous, Partially

Interventions

This is a two-arm, randomized controlled clinical trial, double-blinded (patient and statistician). A randomization sequence will be generated using an online platform (randomization.com) by a researc

Sponsors

Departamento de Odontologia da Universidade Federal de Santa Catarina
Lead Sponsor
Departamento de Odontologia da Universidade Federal de Santa Catarina
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Partially edentulous adult patients; minimum age of 18 years; with horizontal alveolar bone deficiency (less than 4 mm in thickness), confirmed by Cone-Beam Computed Tomography (CBCT); with adjacent teeth to the bone defect areas, in an edentulous space of no more than two missing teeth; adequate oral hygiene (plaque index of 25% or less); no history of bone augmentation procedures in the edentulous area; both sexes

Exclusion criteria

Exclusion criteria: Uncontrolled systemic and local conditions, such as uncontrolled diabetes; pregnant women; smokers; extraction sites with less than 3 months of healing

Design outcomes

Primary

MeasureTime frame
To assess the linear bone gain in millimeters using cone beam computed tomography 6 months after surgery

Secondary

MeasureTime frame
To assess patient-reported outcome measures through questionnaires regarding postoperative recovery, morbidity, surgical time, and incidence of complications after 1 week and 6 months following surgery

Countries

Brazil

Contacts

Public ContactGabriel Magrin

Universidade Federal de Santa Catarina

glmagrin@gmail.com+55 48 3721-9077

Outcome results

None listed

Source: REBEC (via WHO ICTRP)