Accuracy of Tooth Modified Scan Bodies as a Novel Technique
NCT ID: NCT06177782
Last Updated: 2023-12-20
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
60 participants
INTERVENTIONAL
2023-01-10
2023-11-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
I
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Trueness of Full Arch Scans and Generated Digital Implant Models
NCT06281002
Digital Versus Conventional Impression Technique in Mandibular Arch
NCT05770011
Comparing Scanning Accuracy of Full-Arch Maxillary Implants: Extraoral vs. Intraoral Techniques
NCT06669065
Complete Digital Workflow for Construction of Full Arch Implant Supported Screw Retained Restoration
NCT06067334
Digital Intraoral Scanning With and Without Prefabricated Landmarks Versus Conventional Impression Technique
NCT06592066
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.
NON_RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Tooth Modified Scan Bodies
The intraoral scanner (IOS) impression will be recorded using modified scan bodies. The IOS device will be calibrated right before the impression. The scan strategy will be consistent for all the procedures following the manufacturer guidelines.
Tooth modified scan bodies
Tooth modified scan bodies are used during scanning for full arch implant cases.
Conventional Scan Bodies
The intraoral scanner (IOS) impression will be recorded using conventional implant scan bodies secured at the multiunit abutment level.
Conventional scan bodies
Conventional scan bodies will be used for scanning the full arch implant cases.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Tooth modified scan bodies
Tooth modified scan bodies are used during scanning for full arch implant cases.
Conventional scan bodies
Conventional scan bodies will be used for scanning the full arch implant cases.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Participants with 1-piece implant-supported complete-arch fixed dental prostheses.
* Systemically free.
* Primary implant stability exceed 72 the day of the definitive impression.
Exclusion Criteria
* Non co-operative patients.
25 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assiut University
OTHER
Ain Shams University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Doaa Adel Salah Khattab
Associate Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ain Shams University
Cairo, Abbassia, Egypt
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Eldabe AK, Adel-Khattab D, Botros KH. Trueness of tooth modified scan bodies as a novel technique for edentulous full arch implant supported dental prosthesis: an in vivo prospective comparative study. BMC Oral Health. 2025 Jan 6;25(1):29. doi: 10.1186/s12903-024-05172-y.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
22859
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.