- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05436158
The Use of a New Safe Angle Position for Implant Placement in the Anterior Region.
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
Status
Intervention / Treatment
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
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Nesma M Shemais, PhD
- Phone Number: 01005615697
- Email: nesma.shemais@dentistry.cu.edu.eg
Study Contact Backup
- Name: Noha A Ghallab, PhD
- Email: noha.ghallab@dentistry.cu.edu.eg
Study Locations
-
-
Maadi
-
Cairo, Maadi, Egypt, 11728
- Recruiting
- International Dental Continuing Education
-
Contact:
- Ahmed I Abou- El-Fettouh, MSc
- Email: ahmedkey7@hotmail.com
-
Contact:
- Nael A Mina, BDS
-
-
Manial
-
Cairo, Manial, Egypt, 35855
- Recruiting
- Faculty of Dentistry, Cairo University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with immediate implants in the anterior region
- Patient with preoperative and postoperative CBCT
- Provide informed consent.
Exclusion Criteria:
- patients without a preoperative CBCT.
- 2- patients without an informed consent.
Study Plan
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
Sponsor
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
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
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
Other Study ID Numbers
- IDCE.N2
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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