Comparative Assessment of Primary Stability by Osseodensification Using Densah Burs Conventional Drilling Methods.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: osseodensification using densah burs, convetional Driiling technique.
- Who it may be relevant to
- Registry conditions: Patient With Low Denisty Bone. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This clinical study evaluates and compares the primary stability of dental implants placed using osseodensification with Densah burs versus conventional drilling methods. The goal is to determine whether osseodensification improves implant stability and bone density, especially in areas with low bone quality
Interventions
- Procedure osseodensification using densah burs
Participants will be divided into two groups. The first group will undergo implant site preparation using the osseodensification technique with Densah burs, which compacts bone and enhances primary stability without removing bone. The second group will undergo conventional drilling, where bone is removed in a stepwise manner to prepare the implant site according to standard surgical protocols." - Procedure convetional Driiling technique
"This group will receive implant site preparation using the conventional drilling technique, where bone is gradually removed to create space for the implant, as per standard implantology protocols."
Primary outcome measures
- Primary Implant Stability Measured by Implant Stability Quotient (ISQ) Using the Osstell Device [Time frame: Immediately after implant placement (within minutes)]
Eligibility criteria
Inclusion criteria
- Male and female patients
- Patients requiring dental implant placement in areas with varying bone quality
- Patients without systemic diseases that interfere with bone healing or implant success (e.g., uncontrolled diabetes mellitus or osteoporosis)
Exclusion criteria
- Patients with systemic diseases affecting bone metabolism
- Presence of large periapical radiographic lesions related to the tooth to be extracted (abscess, granuloma, or cyst)
- Teeth requiring transalveolar extraction
- Patients with contraindications to surgical treatment
- Patients with psychological disorders
- Patients with uncontrolled medical conditions
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07586475 · 1003/2025