ClinicalTrials.Veeva

Menu

Comparison of Osseodensification and Conventional Drilling on the Stability of Tapered and Cylindrical Implants.

W

Worood Adnan Akram

Status

Active, not recruiting

Conditions

Tooth Absence

Treatments

Procedure: Dental Implant Placement with Osseodensification or Conventional Drilling

Study type

Interventional

Funder types

Other

Identifiers

NCT07244185
974124-2024

Details and patient eligibility

About

The effect of osseodensification versus conventional implant site preparation on implant stability for tapered and cylindrical dental implants.

Full description

Dental implant stability is a key factor influencing the success of osseointegration and the long-term prognosis of implant-supported restorations. The stability of an implant can be divided into two phases: primary stability, which depends on the mechanical engagement between the implant and the surrounding bone at the time of placement, and secondary stability, which develops through biological bone remodeling and osseointegration over time.

Traditional (conventional) drilling techniques used for implant site preparation are subtractive in nature, meaning they remove bone to create space for the implant. However, this process may reduce bone density at the osteotomy walls, particularly in low-density bone, potentially compromising initial stability.

Osseodensification (OD) is a relatively new, non-subtractive drilling technique introduced by Huwais and colleagues. Instead of removing bone, OD uses specially designed, counterclockwise rotating burs (Densah burs) that laterally compact and densify bone along the walls of the osteotomy.

mplant macrodesign-particularly whether the implant is tapered or cylindrical-also influences stability outcomes.

Tapered implants typically provide higher primary stability due to their wedging effect and better adaptation in underprepared osteotomies, especially in soft bone.

Cylindrical implants, while providing more uniform stress distribution, may rely more heavily on bone density and precise site preparation for achieving optimal stability.

Enrollment

36 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 1-Patients who are willing to comply with the study and give their consent. 2-Ability to tolerate conventional surgical and restorative procedure. 3- Healthy patients over 18 years of either gender, having single or multiple missing teeth in the maxilla and/or mandible

Exclusion criteria

  1. Active infection or inflammation in implant area or neighboring zone.
  2. Systemic conditions (medically compromised patient) such as uncontrolled diabetes, coagulation disorders, immune compromised patient, patient treated with bisphosphate drugs, psychiatric problems or unrealistic expectations, pregnant women, any medical condition that affect bone healing.
  3. Clinical evidence of parafunctional habits.
  4. Active periodontitis.
  5. Heavy smokers (≥20 cigarettes a day).
  6. Advanced and complicated cases.
  7. Patients who not able to follow the treatment protocol or lost during the study period.
  8. Patient with history of radiotherapy to the head and neck -

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

36 participants in 4 patient groups

tapered implant with conventional preparation
Experimental group
Description:
The osteotomy will be performed following the manufacturer's standard drilling sequence without osseodensification. This group will serve to evaluate the effect of conventional implant site preparation on the primary and secondary stability of tapered implants
Treatment:
Procedure: Dental Implant Placement with Osseodensification or Conventional Drilling
tapered with osseodensification
Experimental group
Description:
The osteotomy will be prepared with densifying burs operated in a non-subtractive, counterclockwise direction to compact and preserve bone tissue. This approach aims to enhance bone density and improve the primary and secondary stability of the tapered implants
Treatment:
Procedure: Dental Implant Placement with Osseodensification or Conventional Drilling
cylindrical implant with conventional preparation
Experimental group
Description:
The osteotomy will be performed following the standard sequential drilling protocol recommended by the manufacturer, without applying osseodensification. This group will be used to assess the effect of conventional implant site preparation on the primary and secondary stability of cylindrical implants
Treatment:
Procedure: Dental Implant Placement with Osseodensification or Conventional Drilling
cylindrical with osseodensification
Experimental group
Description:
The osteotomy will be performed using densifying burs in a non-subtractive, counterclockwise direction, which compacts and preserves the surrounding bone tissue. This method is intended to increase bone density and improve both primary and secondary implant stability for cylindrical implants
Treatment:
Procedure: Dental Implant Placement with Osseodensification or Conventional Drilling

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems