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Clinical Trial Summary

The aim of this comparative RCT is to evaluate the differences between the entire digital, the combined digital-analogic and the entire analogic workflows of implant-supported and teeth-supported prostheses. It is a three-arms comparative study. The 60 patients are divided into three groups: - fully digital workflow - combined digital and conventional workflow - fully conventional workflow For each patients were evaluated the interproximal (IC) and occlusal contact (OC) and impression time (IT) and the patient satisfaction through a VAS scale. The null hypothesis is that are no differences between the three groups for each parameter.


Clinical Trial Description

This comparative RCT aims to evaluate the differences between the entire digital, the combined digital-analogic, and the entire analogic workflows of implant-supported and teeth-supported prostheses. It is a three-arms comparative study to better focus on the reliability of digital techniques. Inclusion criteria were good oral health, absence of parafunction, no dental caries or presence of periodontitis, and healthy general conditions. Exclusion criteria were bad oral health, parafunctions, dental caries or periodontitis, and general health comorbidities that don't allow surgical treatment. The 60 patients are divided into three groups: - fully digital workflow: each patient in this group was treated with an exclusively digital workflow, from digital planning of the surgical phase to digital impression and digital manufacturing of prosthetic crowns. - combined digital and conventional workflow: each patient of this group was subjected to digital planning, and then, the impressions were taken with traditional analogical materials, so the plaster model was converted into a digital model, and there finally was performed a digital manufacturing of prosthetic crown. - entirely conventional workflow: each patient was treated with an analogical technique. No digital phase was performed. After prosthetic delivery, each patient were evaluated for interproximal (IC) and occlusal contact (OC), impression time (IT), and patient satisfaction through a VAS scale. The null hypothesis is that there are no significant differences between the three groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06215781
Study type Interventional
Source Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Contact
Status Completed
Phase N/A
Start date January 7, 2018
Completion date December 1, 2023

See also
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