Comparative Assessment of Primary Stability by Osseodensification Using Densah Burs Conventional Drilling Methods.

N/ANot Yet RecruitingNCT07586475

Suez Canal University20 enrolled

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

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Patient With Low Denisty Bone

Interventions

osseodensification using densah bursPROCEDURE

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."

convetional Driiling techniquePROCEDURE

"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."

Eligibility

Sex: ALLHealthy volunteers:

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

Primary Implant Stability Measured by Implant Stability Quotient (ISQ) Using the Osstell Device

Description: Primary implant stability will be assessed immediately after implant placement using the Implant Stability Quotient (ISQ) obtained from the Osstell device. The ISQ scale ranges from 1 to 100, with higher values indicating greater implant stability.

Time frame: Immediately after implant placement (within minutes)

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.