Jaw Tracking Impact on Occlusion and Patient Outcomes in Maxillary Implant Restorations
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-70
SponsorMansoura University
About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Conventional Prosthetic Workflow
- Digital Jaw-Tracking Workflow
Treatment groups
20 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov