Accuracy of Guided Implant Placement Using Artificial Intelligence Segmentation Versus Convention… (NCT06967090) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Accuracy of Guided Implant Placement Using Artificial Intelligence Segmentation Versus Conventional Technique
20 participantsStarted 2025-06-01
Plain-language summary
To compare the accuracy of surgical guided implant using AI tooth segmentation of the CBCT alone without intraoral scan to fabricate the implant guide versus conventional technique by alignment the CBCT and intraoral scan to fabricate the implant guide in posterior implant.
Who can participate
Age range
18 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Patients with missing posterior teeth require implant surgery.
. Patients have remaining teeth that can support the surgical guide.
. The edentulous area should involve healed bone sites at least 3 months after extraction.
. The edentulous area should have bone height of at least 10 mm from the alveolar crest to the nearest vital structure and bone width of at least 6 mm.
. Age: patient above 18 years old.
. All patients are in good health with no systemic, immunologic or debilitating diseases that could affect normal bone healing.
. All selected patients are non-smokers and non-alcoholics. Patients are free from temporomandibular disorders and abnormal (TMD) oral habits such as bruxism.
Exclusion criteria
. Systemic disease that may affect bone quality.
. Patients with poor oral hygiene and active periodontal diseases.
. Patient with limited mouth opening.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The accuracy of the placed implants
Timeframe: one week after surgery
2
Horizontal apex deviation, (Measuring unit in millimeter)