Clinical Trial

Artificial Intelligence-Guided Versus Manual CBCT Planning for Immediate Implant Placement

Study acronym: AI
Not Yet Recruiting
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Record status
This record was last updated March 9, 2026 (before its estimated April 2, 2026 completion). Its status may not reflect the trial's current state.
Summary
This study evaluates whether artificial intelligence (AI)-based analysis of cone-beam computed tomography (CBCT) scans can support clinical decision-making for immediate dental implant placement in molar extraction sites. When a molar tooth is removed, placing a dental implant immediately may reduce treatment time and preserve surrounding bone. However, immediate implant placement is not always possible and depends on the anatomy of the extraction socket, particularly the interradicular septum (the bone between the roots). CBCT imaging is routinely used to assess this anatomy before surgery. Traditionally, radiologists manually evaluate these scans. Recently, AI-based tools have been developed to automatically analyze CBCT images. In this randomized controlled trial, patients requiring molar extraction and potential immediate implant placement will be assigned to one of two planning approaches: AI-guided CBCT assessment or conventional manual CBCT assessment. The operating surgeon will use the assigned planning report to guide treatment decisions. The primary outcome of the study is the feasibility of immediate implant placement, defined as successful implant placement with achievement of primary stability during surgery. Secondary outcomes include surgical time, need for changes to the treatment plan, and implant stability measurements. The goal of this study is to determine whether AI-assisted CBCT analysis performs similarly to, or improves upon, conventional manual radiologic assessment in supporting safe and effective immediate implant placement.
Trial Details
NCT Number NCT07459036
Lead Sponsor Shalash Dental education
Conditions Dental Implant, Immediate Implant, Guided Bone Regeneration
Enrollment 80 participants
Start Date 2026-03-03
Primary Completion 2026-04-02 (estimated)
Study Completion 2026-05-02 (estimated)
Updated on ClinicalTrials.gov 2026-03-09