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Complete Digital Workflow for Construction of Full Arch Implant Supported Screw Retained Restoration

Complete Digital Workflow for Construction of Full Arch Implant Supported Screw Retained Restoration :occlusal Accuracy of Different Techniques Used to Record Maxillo-mandibular Relationship(Crossover Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06332482
Enrollment
10
Registered
2024-03-27
Start date
2023-03-30
Completion date
2024-12-20
Last updated
2025-01-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prosthesis Durability

Brief summary

This study will compare the occlusal accuracy of different techniques for recording maxillomandibular relationships in a Complete digital workflow to construct full arch implant-supported screw-retained restoration.

Interventions

DEVICEImplant supported screw retained prosthesis

All patients will receive six maxillary and mandibular implants for full arch screw retained prosthesis

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

digital impressions will be made for each patient,3 technique will be used to determine intermaxillary relation. Occlusal prematurties of final prosthesis will compared using occlusense device and all patients will be followed up for one year

Eligibility

Sex/Gender
ALL
Age
45 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* • Inclusion criteria: i- complete maxillary and mandibular edentulous arches ii- residual alveolar ridges covered with healthy firmly attached mucosa. iii- Angel's class I maxillo-mandibular relationship and iv- Adequate bone height and width for placement of standard diameter implants.

Exclusion criteria

* History of drug administration that interfere with bone quality ii- Surgical contraindication (patients under anticoagulant ,immunosuppressive drugs, chemotherapy and irradiation therapy) iv- tempromandibular or myoneurological disorders.

Design outcomes

Primary

MeasureTime frameDescription
measurement of occlusal prematurityone yearOcclusal prematureties of final prosthesis will be measured using occlusense device
prosthestic complicationsone yearprosthetic complications will be recorded for all patients and statistically analyzed

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026