RecruitingNot Applicable

Jaw Tracking Impact on Occlusion and Patient Outcomes in Maxillary Implant Restorations

Egypt20 participantsStarted 2025-12-25

Plain-language summary

This randomized clinical trial aims to evaluate the effect of integrating digital jaw tracking into the workflow for fabrication of full-arch maxillary implant-supported screw-retained restorations. Twenty completely edentulous maxillary patients opposing natural mandibular dentition will be randomly assigned to either a conventional workflow group or a digital jaw-tracking workflow group. The study will compare patient satisfaction and occlusal accuracy between the two groups. Patient satisfaction will be assessed using a visual analogue scale (VAS), while occlusal accuracy will be evaluated using the OccluSense system.

Who can participate

Age range

50 Years – 70 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: * Male or female patients aged 50 to 70 years. * Completely edentulous maxillary arch opposing natural mandibular dentition. * Skeletal Class I maxillomandibular relationship with normal occlusion. * Acceptable oral hygiene. * Willing and able to provide written informed consent and comply with study procedures. Exclusion Criteria: * Systemic diseases affecting bone healing, such as uncontrolled diabetes mellitus or osteoporosis. * Harmful oral habits, including smoking, clenching, or bruxism. * Uncooperative patients or patients unable to comply with study procedures.

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

Patient Satisfaction

Timeframe: At prosthesis insertion, 3 months, and 6 months after prosthesis insertion

Trial details

NCT IDNCT07693946

SponsorMansoura University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12-25

Contact for this trial

Shahira s Mohamed, BDS

+20 1004455178 shahirasaad@mans.edu.eg

View on ClinicalTrials.gov More Edentulism trials