Complete Maxillary Edentulism, Edentulism
Conditions
Keywords
Digital jaw tracking, Maxillary implant-supported prosthesis, Screw-retained prosthesis, Occlusal accuracy, Patient satisfaction, OccluSense, Randomized clinical trial
Brief 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.
Detailed description
This randomized clinical trial will compare conventional prosthetic workflow with a digital jaw-tracking workflow for the fabrication of full-arch maxillary implant-supported screw-retained restorations. Twenty edentulous patients with completely edentulous maxillary arches opposing natural mandibular dentition will be recruited and randomly allocated into two equal groups. Group A will receive restorations fabricated using the conventional workflow with static jaw relation records, while Group B will receive restorations fabricated using a digital workflow incorporating dynamic jaw tracking and a virtual articulator. The primary outcome will be patient satisfaction, assessed using a visual analogue scale (VAS) after prosthesis insertion and during follow-up visits. Occlusal accuracy will be evaluated using the OccluSense digital occlusal analysis system. The study aims to determine whether digital jaw tracking improves occlusal accuracy and patient-reported outcomes compared with the conventional workflow.
Interventions
Fabrication of a full-arch maxillary implant-supported screw-retained prosthesis using conventional jaw relation records, a facebow or average-value articulator, and conventional occlusal adjustment procedures.
Fabrication of a full-arch maxillary implant-supported screw-retained prosthesis using a digital workflow with dynamic jaw tracking, virtual articulator integration, and CAD/CAM technology for patient-specific occlusal design.
Sponsors
Study design
Intervention model description
Participants will be randomly assigned to one of two parallel groups: a conventional workflow group or a digital jaw-tracking workflow group.
Eligibility
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Patient Satisfaction | At prosthesis insertion, 3 months, and 6 months after prosthesis insertion | Patient satisfaction will be assessed using a Visual Analogue Scale (VAS) to evaluate patient satisfaction with the implant-supported prosthesis regarding comfort, chewing ability, aesthetics, and phonetics. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Occlusal Accuracy | At prosthesis insertion and 3 months after insertion | Occlusal accuracy will be evaluated using the OccluSense digital occlusal analysis system by assessing the distribution and stability of occlusal contact points. |
Countries
Egypt
Contacts
Faculty of Dentistry, Mansoura University