Assessment of the Accuracy of Full Digital Workflow in Patient Specific Submerged Subperiosteal Implants: A Case Series Study
NCT ID: NCT07014527
Last Updated: 2025-06-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
10 participants
INTERVENTIONAL
2025-01-01
2025-05-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Complete Digital Workflow for Construction of Full Arch Implant Supported Screw Retained Restoration
NCT06332482
Trueness of Full Arch Scans and Generated Digital Implant Models
NCT06281002
Two Versus Four Implant-supported Fixed Full-arch Prosthesis
NCT05290766
Complete Digital Workflow
NCT07091786
Complete Digital Workflow for Construction of Full Arch Implant Supported Screw Retained Restoration
NCT06067334
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Computer guided custom made subperiosteal implant treatment
Patients will receive a patient specific custom made subperiosteal implant and the accuracy will be assessed
Patient specific subperiosteal implants
Patient specific subperiosteal implants
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Patient specific subperiosteal implants
Patient specific subperiosteal implants
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cairo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Mohamed Shawky
Assistant lecturer
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Faculty of dentistry, Cairo University
Cairo, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OMFS 2025
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.