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

ConditionPatient With Low Denisty Bone

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

AgeNot listed

SponsorSuez Canal University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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)

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

osseodensification using densah burs
Procedure/Surgery
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 technique
Procedure/Surgery
"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."

Treatment groups

20 Participants

are divided into 2 treatment groups

Group A: controlled group conventional drilling groupActive comparator 1 intervention

Group B: study group of osseodensification GroupExperimental treatment 1 intervention

Trial 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)

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Suez Canal University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: