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Clinical Trials/NCT06667778
NCT06667778
Completed
N/A

Effectiveness of Osseodensification in Enhancing Implant Stability and Ridge Expansion in Esthetic Region (a Randomized Controlled Clinical Trial)

Hams Hamed Abdelrahman1 site in 1 country18 target enrollmentJanuary 12, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dental Implant
Sponsor
Hams Hamed Abdelrahman
Enrollment
18
Locations
1
Primary Endpoint
Change in implant stability
Status
Completed
Last Updated
last year

Overview

Brief Summary

Dental implants supported restorations have been widely accepted as one of the treatment modalities to replace missing teeth and to restore human masticatory function. Successful osseointegration from the clinical standpoint is a measured by implant stability, which occurs after implant integration. Osseodensification is a bio-mechanical site preparation technique. It utilizes a multi-fluted densifying bur technology that creates and expands a pilot hole without excavating significant amounts of bone tissue through a unique, highly controllable, fast, and efficient procedure with minimal heat elevation.

Aim of the study: Is to evaluate and compare the efficacy of using osseodensification compared to conventional bone expansion in implant stability and ridge expansion.

Registry
clinicaltrials.gov
Start Date
January 12, 2021
End Date
September 28, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hams Hamed Abdelrahman
Responsible Party
Sponsor Investigator
Principal Investigator

Hams Hamed Abdelrahman

Assistant Lecturer of Dental Public Health and biostatistical consultanat

Alexandria University

Eligibility Criteria

Inclusion Criteria

  • Missing maxillary anterior tooth, having moderate horizontal ridge defect in which the alveolar ridge width is( 3-4) mm, and its height is not less than 10 mm.
  • Presence of adequate keratinized mucosa.
  • Patients with good oral hygiene.
  • Patients are free from any systemic diseases that might affect healing.
  • Presence of adequate inter-occlusal and mesiodistal space that permits placement of fixed prosthesis.

Exclusion Criteria

  • Heavy smokers and bad oral hygiene patients.
  • Medically compromised patients that affecting placement of implant.
  • Alcohol or drug abuse.
  • Pregnant women.
  • Patients suffering from osteoporosis.
  • Current chemotherapy or radiotherapy.

Outcomes

Primary Outcomes

Change in implant stability

Time Frame: Baseline and 16 weeks

Implant stability will be measured using the Ostell device.

Secondary Outcomes

  • Change in bone density(Baseline and 16 weeks)
  • Change in ridge expansion(Baseline and 16 weeks)
  • Change in bone loss(Baseline and 16 weeks)

Study Sites (1)

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