- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07378020
Comparing Between Osseodensification Burs Versus Osteotome in Low Bone Density Areas. (osseo-1)
A Comparative Study of Osseodensification Burs Versus Osteotome Preparation on the Stability of Implants Placed in Low Bone Density Areas: a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
in different conditions implants that lack primary stability is subjected to excessive micromotion that can lead to implant failure. This usually happens when dental implants pass the critical limit of micro-motion. Passing this critical limit can interfere with Osseo-integration and cause fibrous encapsulation of dental implant .
Implant Failure usually occurs in completely edentulous maxillae especially in the posterior area where bone quality is compromised.
Clinicians usually refer implants success rates to the difference in bone quality between mandible and maxilla. Higher failure rates seem to be associated with poor bone quality.
Primary stability is affected by several factors including Bone Quantity and quality, the Implant macro- and micro- design, and the used osteotomy technique.
Osteotomies are usually created using conventional drills, although the implant diameter must be slightly larger than the final drill to ensure primary stability However, this conventional drilling technique might be insufficient to provide the primary stability required for Osseo-integration in areas of low bone quality. Several site preparation techniques have been introduced to enhance primary stability in soft bone. Some clinicians used under-sized drilling however the efficiency of this technique is conditioned by decreasing osteotomy diameter by 10% of implant diameter.
Another method introduced by Dr. Robert Summer. This method uses bone condensers to densify bone through the condensation and expansion of spongy bone as it squeezes bone trabeculae laterally against the wall of implant bed at the site of osteotomy increasing the bone density and conserving osseous tissue around implants.
Recently Osseodensification (OD) was introduced as a novel implant site preparation technique that uses specially designed drills with large negative rake angles. When the drills are operated in a counterclockwise direction it acts as a non-cutting drill which is used to expand and compact bone against the osteotomy walls. This non-subtractive approach aims to increase the primary stability of the dental implants inserted into low-density bone compared with conventional drilling techniques. The drills also can be used as a cutting drill when operated in a clockwise direction according to the operator's need. This type of drill can improve bone density leading to improved implant primary stability, giving these drills the ability to cut and densify without the need for additional tools.
Ossoe-densification technique showed greater insertion torques, bone-to implant contact, and bone area fraction occupancy when compared to standard Drilling technique.
this study is comparing between the three different drilling techniques (conventional, osseo-densification, osteotome bone compaction) in enhancing insertion torque and isq values in posterior maxillary area.
the study also compare between the effect of these techniques on marginal bone loss with follow up 6 month after loading using cbct
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Fifth Settlement
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Cairo, Fifth Settlement, Egypt, 11835
- Oral and Maxillofacial Department Future Dental Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients with low bone density (D3), (D4) Missing maxillary posterior teeth
- edentulous ridge should be 8 mm or more of bone height and bone width ≥ 7mm with adequate inter-occlusal space of at least 8mm,
- Patients with good oral hygiene or willing to improve their oral hygiene.
Exclusion Criteria:
- Patients with uncontrolled medical conditions that affect Osseo-integration.
- Patients receiving medications that contraindicate osteotomy.
- Heavy smokers.
- History of receiving irradiation in the head and neck region.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: Conventional Drilling
Implant sites in this arm will undergo osteotomy preparation using standard conventional drilling sequences according to the implant manufacturer's recommendations prior to implant placement
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The implant site will be prepared using a standard sequence of drills (subtractive osteotomy) according to the implant manufacturer's instructions.
Drilling will be performed with profuse irrigation at speed between 800-1200 rpm to remove bone and prepare the osteotomy site to the final diameter before implant insertion
Other Names:
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Experimental: Densah Bur (Osseodensification)
Implant sites in this arm will undergo osteotomy preparation using the osseodensification technique with Densah burs (Versah) running in a counter-clockwise direction (densifying mode) prior to implant placement.
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after using the pilot drill in a clockwise direction to drill to the desired depth according to the planned implant length The implant site will be prepared using Densah burs (Versah).
the motor is adjusted to rotate in a counter-clockwise direction (densifying mode) at 800-1200 rpm with profuse irrigation.
This technique expands the osteotomy site by compacting bone at the periphery rather than removing it, aiming to enhance bone density around the implant then the implant is inserted after reaching the desired diameter according to densah bur soft bone drilling protocol
Other Names:
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Experimental: osteotome
Implant sites in this arm will undergo osteotomy preparation using summers osteotome technique for lateral bone condensation and expansion prior to implant placement
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osteotomy was prepared using (Xive BoneCondensers by dentsply sirona GERMANY) starting from the pilot drill of 1.7mm in diameter to penetrate the cortical bone and gain access.
Then instrumentation was done in the following sequence: 2.0mm, 3.0mm, and 3.4mm according to the planned implant diameter.
The osteotome was inserted manually and rotated while being pressed towards the apical part of osteotomy till it reaches the full working depth.
Once the desired depth was reached, and before moving to the next instrument we wait 1 min for the osteotome to compress and compact the spongy bone.
After the implant bed had been prepared, we inserted the implant immediately to avoid any dimensional changes in the site of osteotomy.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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primary stability using Insertion Torque Value.
Time Frame: day of surgery
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Evaluation of implant stability was done by measuring Insertion torque.
Using the surgical contra-angled hand piece the initial torque value was set to10Ncm then increased sequentially by 5Ncm according to the torque required to place the implant at the desired depth.
The final torque value used to drive the implant to its position was recorded as the peak insertion torque
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day of surgery
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Primary Implant Stability measured through Resonance Frequency Analysis (RFA)
Time Frame: the day of surgery
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Implant stability will be measured using Resonance Frequency Analysis (RFA) via an Osstell device.
The values are recorded as Implant Stability Quotient (ISQ) on a scale from 1 to 100, where higher scores indicate greater stability
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the day of surgery
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Secondary Implant Stability using radio frequency analysis (RFA)
Time Frame: readings were taken 3 months post operative and 6 months after loading.
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Implant stability measured using Resonance Frequency Analysis (RFA) via Osstell.
Values recorded as ISQ (1-100) to evaluate osseointegration.
where higher scores indicates higher stability
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readings were taken 3 months post operative and 6 months after loading.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Marginal Bone Loss (MBL)
Time Frame: cbct was done at implant placement and 3 months post operative and 6 months after loading.
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Radiographic evaluation of crestal bone changes measured using cone beam CT.
The difference in bone level between baseline and follow-up will be calculated in millimeters.
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cbct was done at implant placement and 3 months post operative and 6 months after loading.
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: dr lobna abdelaziz aly, PhD, Future University in Egypt
Publications and helpful links
General Publications
- Elsheikh HA, Gadallah AT, Kandil I. Impact of Three Different Surgical Drilling Protocols on Early Loaded Single Implant in Posterior Maxilla: A 3-year Follow-up. J Contemp Dent Pract. 2022 Aug 1;23(8):819-827.
- Evrenk O, et al. Evaluation of implant primary stability using different drilling protocols: an in vitro study. BMC Oral Health. 2025 Aug 9. doi: 10.1186/s12903-025-06661-4.
- Huwais S, Meyer EG. A Novel Osseous Densification Approach in Implant Osteotomy Preparation to Increase Biomechanical Primary Stability, Bone Mineral Density, and Bone-to-Implant Contact. Int J Oral Maxillofac Implants. 2017 Jan/Feb;32(1):27-36.
- Summers RB. A new concept in maxillary implant surgery: the osteotome technique. Compend Contin Educ Dent. 1994 Feb;15(2):152, 154-6, 158 passim.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUE.REC (25)/7-2023
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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