Assessment of the Accuracy of Surgical Guide Designed From Digital Impression, Dental Model Scanning Using CBCT and Desktop Scanner in Computer Guided Implantology:
NCT ID: NCT03730506
Last Updated: 2018-11-05
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.
UNKNOWN
NA
9 participants
INTERVENTIONAL
2018-11-30
2020-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Randomized Clinical Trial.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Accuracy of CBCT Imaging and Intraoral Scanner in Dental Plaster Casts Digitization: A Validity and Reliability Study
NCT05817552
Evaluation of the Accuracy of Digital Models Obtained Using Intraoral and Extraoral Scanners
NCT03103802
Accuracy in Computer Guided Versus Free Hand Immediate Implantation
NCT03281148
Automatic Versus Semiautomatic Registration of Digital Dental Cast to Cone Beam Computed Tomography Image
NCT04563117
Computer Guided Versus Free Hand Immediate Implant Placement
NCT03230500
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
In computer guided Implantology, are surgical stents designed from scan of dental model by CBCT and from digital impression as accurate as surgical stents designed from desktop scanner?
Statement of the problem:
The role digital dentistry is improved in computer guided implantology especially with development of computer guided implant software, desktop scanner and intra oral scanner development and CBCT machines.
Intra-oral scanner, desktop scanner and CBCT scanner can be used in creation of 3D digital model that can be used with computer guided implant in fabrication of the surgical stent.
And the question, is the accuracy of surgical guide will be affected when designed by one of these different modalities?
Rationale for conducting the research:
Digital 3D dentoginival details are very important in computer guided implantology and designing of surgical stent.nowadays there are many methods to obtain this soft tissue replica as CBCT,desktop scanner and intra oral scanner.this study is conducted to asses the effect of different method of soft tissue digitization on the accuracy of surgical template used in computer guided implantology.
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.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
CBCT
Intra oral scanner
computer guided implant
IOS
Intra oral scanner
computer guided implant
desktop scanner
Intra oral scanner
computer guided implant
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Intra oral scanner
computer guided implant
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients with bucco-lingual bone thickness more than 6 mm allowing flapless implant placement.
Exclusion Criteria
* Patients needing graft or sinus lifting with implant placement.
* Patients with thin ridges.
* Patients with systemic disease that may affect bone quality.
* Patients with poor oral hygiene and active periodontal diseases.
* Patient with limited mouth opening
ALL
Yes
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.
Amr taha Adu el wafa
teaching assistant
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RAD2:7:1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.