RecruitingPhase 4

Artificial Intelligence Assisted Workflow Versus Conventional Workflow in Guided Implant Placement

Egypt20 participantsStarted 2026-05-01

Plain-language summary

The AI assisted CAD/CAM workflow will be adopted for the treatment planning and guide design generation with the aim of comparing precision of implant placement with conventional digital workflow.

Who can participate

Age range

18 Years – 50 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: * Kennedy class III partially edentulous patient with or without modifications. * Patients who need single implant posterior site delayed implant placement. * Patients above 18 and below 60 years of age. * Natural healthy neighboring teeth without need of new restorations. Exclusion Criteria: * Patients with D4 bone density. * Patients with known systemic or local diseases or treatments which can affect normal tissue healing. * Patients who are heavy smokers. * Presence of signs of active infection or pus formation. * Patients with a need for implants in the anterior region. * Additional oral surgery in the region of interest. * Need For Bone grafting. * Pregnant and/or lactating women

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

Linear Discrepancy

Timeframe: Immediate post operative

Angular Discrepancy

Timeframe: Immediate post operative

CAD Timing

Timeframe: Immediate post operative

Trial details

NCT IDNCT07523815

SponsorSandra Moussa Botros El Tarzi

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-10-01

Contact for this trial

Sandra Moussa El Tarzi, BDS

+201226665141 sandra.eltarzi@dentistry.cu.edu.eg

View on ClinicalTrials.gov More Partially Edentulous Mandible trials

Who can participate

Age range

18 Years – 50 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.