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NCT Number: NCT07586475

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

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

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Key information

Conditions

Patient With Low Denisty Bone

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

osseodensification using densah burs

Procedure

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

"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 outcomes

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

Time frame: Immediately after implant placement (within minutes)

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.

Sponsors and collaborators

Lead sponsor

Suez Canal University

Other

Registry information

Important dates

Study start: 2026
Primary completion: 2026
Study completion: 2027
First posted: May 14, 2026
Registry last updated: May 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.