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Comparison Between Conventional and Digital Workflow in Dental Prosthesis

Not Applicable
Completed
Conditions
Dental Prosthesis Complication
Interventions
Procedure: Fully digital workflow of prosthetic fixed dental crown
Procedure: Fully conventional workflow of prosthetic fixed dental crown
Procedure: Combined digital and conventional workflows of prosthetic fixed dental crown
Registration Number
NCT06215781
Lead Sponsor
Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Brief 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.

Detailed 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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • good oral health
  • good general health conditions
  • no contraindication to oral surgery and fixed prosthesis
  • patients who completed the 6 months follow-up
Exclusion Criteria
  • bad oral health
  • bad general health conditions (with multi-drug therapy)
  • periodontitis or dental caries susceptibly
  • parafunctions presence
  • TMJ disorders
  • didn't accept the informed consent / treatment planning

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Fully digital workflowFully digital workflow of prosthetic fixed dental crownPatients of this group are subjected to entire digital workflow, from the digital planning to the delivery of definitive zirconia fixed dental prosthesis
Fully conventional workflowFully conventional workflow of prosthetic fixed dental crownPatients of this group follow the entire analog protocol. All the procedures exclude digital involvement.
Combined digital-conventional workflowsCombined digital and conventional workflows of prosthetic fixed dental crownPatients of this group were subjected to every digital steps as the "fully digital workflow" arm, except for the impression that includes analog material (silicones).
Primary Outcome Measures
NameTimeMethod
Patient satisfaction degree2 weeks after definitive prosthesis delivery

Patient satisfaction through a VAS scale. The patients is asked to make a mark in an unnumbered line ranging from 0 to 5 where 0 represents maximum comfort and 5 represents a very bad experience. The scale is 5 cm long so the clinician next measures the distance (in cm) from 0 to where the mark was placed by the patient.

Entity of occlusal contact2 weeks after definitive prosthesis delivery

The entity of contact between prosthetic crown and antagonist teeth was evaluated with a dichromatic articulating paper in order to identify any static and dynamic alterations in occlusal contacts that must be corrected. The clinician gives a score from 0 to 3 where 0 is the absence of contact between crown and antagonists, 1 is a correct contact between them that needs no corrections, 2 there is a slight altered contact that requires minor corrections and 3 there is an altered contact between the prosthetic crown and their antagonists which requires major corrections.

Impression time2 weeks after definitive prosthesis delivery

Length of time useful to take impression expressed in seconds

Entity of interproximal contact2 weeks after definitive prosthesis delivery

Precision of interproximal contact between prosthetic crown and adjacent teeth. It was measured by the clinician evaluating the resistance to the sliding of waxed dental floss. The clinician gives to the interproximal contact a score from 0 to 4, where 0 is considered as an absence of resistance (open space between crown and adjacent teeth) and 4 is the total impediment to the floss slide (the crown and the adjacent teeth are too close to have a correct interproximal contact)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Massimo Corsalini

🇮🇹

Bari, Italy

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