The Use of a New Safe Angle Position for Implant Placement in the Anterior Region.

June 23, 2022 updated by: Nesma Mohamed Fouad Shemais, Cairo University

The Use of a New Safe Angle Position for Implant Placement in the Anterior Region: A Cross-sectional Study

There is an angle between the intersection of the incisal long axis perpendicular to the palate or the occlusal plane, and the long axis of the root. When this relation is shifted more palatal, where the incisal plane line will be at the cingulum position or slightly palatal to it, it is named the safe angle position. The more palatal relocation to the cingulum is performed according to the availability of palatal bone, the occlusion with the opposing dentition, the type of the restoration (screw vs cemented).

The possibility of having a specific safe angle to place implants opens new interesting perspectives for immediate placement of dental implants.

The aim of the present study was to demonstrate how immediate implants in the safe angle position can be predictably achieve proper implant positioning, better esthetics and emergence profile as well as less stresses on the implant.

Study Overview

Detailed Description

Immediate implants are implants inserted immediately after surgical extraction of the teeth to be replaced. Creation of an anatomically correct emergence profile is one of the most important aspects in providing an esthetically pleasing implant-supported restoration. Dentists understand the risks involved when restored prostheses are subjected to non-axial loading. It has always been recommended to direct occlusal loads as close to the long axis of the fixture as possible. However, it is known that the loading on angled abutments is mostly off-axis, which raises the concern of how angled abutments generally perform with such an unfavourable loading regimen.

There is an angle between the intersection of the incisal long axis perpendicular to the palate or the occlusal plane, and the long axis of the root. When this relation is shifted more palatal, where the incisal plane line will be at the cingulum position or slightly palatal to it, it is named the safe angle position. The more palatal relocation to the cingulum is performed according to the availability of palatal bone, the occlusion with the opposing dentition, the type of the restoration (screw vs cemented).

The possibility of having a specific safe angle to place implants opens new interesting perspectives for immediate placement of dental implants.

The aim of the present study was to demonstrate how immediate implants in the safe angle position can be predictably achieve proper implant positioning, better esthetics and emergence profile as well as less stresses on the implant.

Study Type

Observational

Enrollment (Anticipated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Maadi
      • Cairo, Maadi, Egypt, 11728
        • Recruiting
        • International Dental Continuing Education
        • Contact:
        • Contact:
          • Nael A Mina, BDS
    • Manial
      • Cairo, Manial, Egypt, 35855
        • Recruiting
        • Faculty of Dentistry, Cairo University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with immediate implants in the anterior region

Description

Inclusion Criteria:

  1. Patients with immediate implants in the anterior region
  2. Patient with preoperative and postoperative CBCT
  3. Provide informed consent.

Exclusion Criteria:

  1. patients without a preoperative CBCT.
  2. 2- patients without an informed consent.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
presence of the implant in the safe angle
Time Frame: 6 months
binary (Y/N) from CBCT
6 months
use of angled or straight abutment
Time Frame: 6 months
Binary (straight/angled)
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pink Esthetic Score
Time Frame: 6 months
Pink Esthetic Score (1-14)
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Noha A Ghallab, PhD, Professor of Oral Medicine & Periodontology
  • Principal Investigator: Ahmed I Abou- El-Fettouh, MSc, MIU
  • Principal Investigator: Abdelrahman Zohny, BDs, MIU
  • Principal Investigator: Nael M Adel, BDs, MIU
  • Principal Investigator: Mariam S Abdelmalak, BDs, MIU

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 1, 2022

Primary Completion (ANTICIPATED)

August 1, 2022

Study Completion (ANTICIPATED)

September 1, 2022

Study Registration Dates

First Submitted

June 19, 2022

First Submitted That Met QC Criteria

June 23, 2022

First Posted (ACTUAL)

June 28, 2022

Study Record Updates

Last Update Posted (ACTUAL)

June 28, 2022

Last Update Submitted That Met QC Criteria

June 23, 2022

Last Verified

June 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • IDCE.N2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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