About this trial
This study aims to evaluate the marginal and internal fit of intra-radicular attachments fabricated by direct scanning using two different intraoral scanners compared to indirect scanning of conventional impressions.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Endodontically treated teeth requiring intraradicular attachments.
Adequate oral hygiene.
Partially edentulous cases where compromised remaining teethcannot serve as abutments for traditional removable partial dentures (RPDs). -
Periodontally compromised teeth that can still be maintainedasoverdenture abutments with proper treatment.
Disqualifiers
Severely compromised remaining teeth with poor prognosis duetoextensive decay or severe periodontal disease.
Severe bone loss around abutment teeth.
Severe malocclusion making overdenture placement difficult.
Limited inter-arch space that cannot accommodate overdenturecomponents. 5. Poor oral hygiene increasing the risk of decay or periodontal issues.
Trial design
Crossover
Treatments tested in this trial
conventional impression
Procedure/Surgeryindirect scanning for conventional impression
Intraoral scanner
DeviceUse of an intraoral scanner to obtain digital impressions for the fabrication of intra-radicular attachments. Two different intraoral scanners will be used to capture digital data of the prepared tooth, and the resulting scans will be used to fabricate the attachments through a CAD/CAM workflow. The accuracy of the fit will be evaluated and compared with conventional impression techniques.
Treatment groups
Trial outcomes
Primary outcomes
Marginal and internal fit evaluated using software.
Secondary outcomes
Time control, the time taken for each scanningor impression-taking process will be recorded in seconds using a stopwatch.
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: