- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06012643
Subperiosteal Implants Constructed With Digital Technology
Subperiosteal Implants as a Treatment for Severely Atrophied Jaw in Completely and Partially Edentulous Population: A Systematic Review of Case Reports and Case Series.
Study Overview
Status
Conditions
Detailed Description
An electronic and manual search was conducted in the PubMed, Scopus, and Google Scholar databases. Publications of case reports and series written in English without data restrictions that reported on subperiosteal implants management of patients with severely atrophied jaws in completely and partially edentulous population.
The purpose of this systematic review of case reports and case series was to evaluate the spectrum of subperiosteal implants for severely atrophied jaws using digital technology.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Mohammed Elsawy, PhD
- Phone Number: 00201061314522
- Email: Dr_sawy@windowslive.com
Study Contact Backup
- Name: Salah A. Hegazy, PhD
- Phone Number: 00201227690209
- Email: salahhegazy@yahoo.com
Study Locations
-
-
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Multiple Locations, Egypt, 12345
- Recruiting
- Mohammed El Sawy
-
Contact:
- Mohammed E Sawy, PhD
- Phone Number: +201061314522
- Email: Dr_sawy@windowslive.com
-
Contact:
- Salah A. Hegazy, PhD
- Phone Number: +01227690809
- Email: salahhegazy2003@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- population with partial or fully edentulous arches, in particular Cawood and Howell class (IV-VI);
Exclusion Criteria:
- Articles were excluded if complex reconstructive surgery including bone grafts, barrier membranes, jaw osteotomies, sinus lift, alveolar ridge distraction, and zygomatic implants was recommended for treatment
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
to evaluate the spectrum of subperiosteal implants for severely atrophied jaws using digital technology.
Time Frame: 5 year retrospective
|
The outcome was implant success or rejection.
|
5 year retrospective
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Biological complications
Time Frame: 5 year retrospective
|
such as (dehiscence or exposure of the framework)
|
5 year retrospective
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prosthetic complications
Time Frame: 5 year retrospective
|
such as (fracture of the definitive or temporary prosthesis)
|
5 year retrospective
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mohammed ELSawy, PhD, Mansoura University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- A0107023RP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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