Evaluation of Occlusal Contact Distribution in Digitally Fabricated Implant-Retained Fixed Partial Dentures in Mandibular Kennedy Class II Patients Following Artificial Intelligence Bite Optimization: A Quasi-Experimental Study

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCairo University

About this trial

The aim of the study is to evaluate the occlusal contact distribution in digitally fabricated implant-retained fixed partial dentures in mandibular Kennedy Class II patients before and after artificial intelligence bite optimization.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patients with a unilateral mandibular distal extension area (Kennedy Class II partially edentulous mandibular arch) and who are indicated for the insertion of 2 implants.

Fully dentate opposing maxillary arch or restored with a suitable, well constructed fixed prosthesis.

The remaining teeth should be in good periodontal health, with no signs of inflammation or movement.

The edentulous area should be covered by a healthy, firm mucoperiosteum, with no or minimal tissue undercut.

Disqualifiers

Patients with psychological or mental disorders.

Patients with insufficient interarch space.

Patients with parafunctional habits, such as bruxism.

After the healing phase and exactly before the prosthetic phase, if the inserted implants showed any signs of peri-implantitis or aggressive crestal bone resorption, then this case will be excluded and replaced with another case.

Trial design

Design model

Sequential

Treatments tested in this trial

  • After

    Procedure/Surgery

    The data acquisition will take place by scanning the patients using Medit intraoral scanner. Then, the scanned stls will be imported in 3shape software version 2024 and bite optimization module in it will be run. It automatically recalculates the position of the bite relation using its integrated AI. After that, the resulted STLs will be exported and re-imported to ExoCAD software to design the prostheses.

  • Before

    Procedure/Surgery

    The recruited patients will be screened for proper bone architecture and CBCTs will be taken for proper virtual implant planning. Two implants will be placed in the edentulous span in all participants. All surgical steps will be held according to standard protocol. After the implant osseointegration period, the prosthetic phase will start with implant exposure and placement of multiunit abutments. After gingival healing, intraoral scans for the implants timing using abutment level scan bodies will be taken. Then, the fabrication of implant-retained fixed partial denture will be done with a fully digital workflow.

Treatment groups

15 Participants
are divided into 2 treatment groups
Group A: BeforeExperimental treatment 1 intervention
Group B: AfterActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Occlusal contact distribution

The 1ry outcome will be assessed on the day of the prosthesis delivery. First, the reading of the occlusal contact distribution will be taken by using the T-scan device before seating the prosthesis intraorally. Then, the retained fixed prosthesis will be seated on the implant abutment, and the prosthetic screw will be screwed to the optimum torque. Another reading of the occlusal contact distribution will be taken by using the T-scan device after seating and torquing the prosthesis intraorally. Finally, the screw access channels will be closed by flowable resin composite material.

Time frame
From enrollment till the end of the study 17 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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