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Clinical Trials/NCT04630665
NCT04630665
Completed
N/A

Clinical Assessment of Buccal Bone Resorption in Immediate Implants in Thin and Thick Buccal Plates of Bone and Its Implication on Esthetics. A Controlled Clinical Trial

Cairo University1 site in 1 country18 target enrollmentJanuary 23, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Buccal Bone Thickness
Sponsor
Cairo University
Enrollment
18
Locations
1
Primary Endpoint
buccal bone thickness
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

To achieve esthetic immediate implants a minimum of adequate buccal bone thickness must be present. It was postulated that 2 mm of buccal bone thickness was needed to prevent recession of the buccal plate. However, this was reduced to 1 mm with more ongoing research. In a recent study postulated that a buccal bone thickness less than 1 mm could be sufficient.

Scarce literature was found that monitored the ridge alterations following implant placement.

In regards to the controversies regarding the minimal initial buccal bone thickness required to perform immediate implant placement, our study aims to monitor the buccal bone thickness and soft tissue changes over a year from implant and prosthetic placement.

Registry
clinicaltrials.gov
Start Date
January 23, 2019
End Date
November 2, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Suzy Nabil Naiem

Principal Investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Subjects who have at least one unrestorable tooth in the esthetic zone that needs to be extracted.
  • Subjects with healthy systemic condition.
  • Availability of bone apical and palatal to the socket to provide primary stability.

Exclusion Criteria

  • Patients with signs of acute infection related to the area of interest.
  • Patients with habits that may jeopardize the implant longevity and affect the results of the study such as parafunctional habits.

Outcomes

Primary Outcomes

buccal bone thickness

Time Frame: 1 year

measurement of buccal bone thickness by a specially designed device and cone-beam computed tomography (CBCT) analysis

Secondary Outcomes

  • pink esthetic score (PES)(1 year)

Study Sites (1)

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