Occlusal Adjustment Time and Volume for Single Unit Fixed Prosthesis Fabricated With Different Virtual Mounting

NCT ID: NCT05471024

Last Updated: 2022-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

33 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-01

Study Completion Date

2022-07-27

Brief Summary

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Regardless of the fabrication workflow occlusal adjustments seem to be inevitable during delivery of indirect fabrication of the restoration. This has been attributed to snowballing of discrepancies due to multiple procedures for information transfer between the clinician and the laboratory. Current digital workflows minimize these discrepancies due to digital acquisition technology which eliminates drawbacks from physical materials which would alter the dimensions and morphology of the final restoration. Utilizing 3D face scanning technology is by far the least invasive and the least time consuming of available virtual facebow techniques and thus it's utilization could offer the benefit of saving time during occlusal adjustment and enhanced strength of the restoration by not subjecting it to the heat generation and subsequent crack initiation which occurs during occlusal adjustment. This study aims to compare the effect of a face scan to alignment of the maxillary cast on the volume and time of occlusal adjustment compared to conventional articulator digitization to align the maxillary cast.

Detailed Description

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This study will be carried out on participants enrolled at the outpatient fixed prosthodontics clinic, Faculty of Dentistry, Cairo University.

Digital face scanning technology has made it possible to align the maxillary cast in a virtual articulator to represent a more accurate relationship to the terminal hinge axis of the patient than average positioning on a virtual Bonwill triangle. This would be reflected on the occlusal design of the restoration and subsequently on the amount of adjustment needed to the occlusal surface of the restoration during delivery. Decreasing the amount and time of occlusal adjustment would result in a decrease in chair time, increase in the longevity of the restoration and enhanced esthetics of the restoration.

Conventional alignment and mounting of casts to simulate the patients' dynamic occlusions remains the gold standard to which newer digital cast alignment and relation technology is to be compared. Thus the selection of the articulator scan as the comparator was made

Participants' Timeline

Clinical Visit 1 Preoperative records Clinical examination, Radiographic examination, Assessment of inclusion, Informed consent, Intraoral photographs, Primary impression (irreversible hydrocolloid) for diagnostic cast fabrication.

Clinical Visit 2 Facebow record, Articulator mounting, Face Scan, Foundation restoration for participant tooth built to full contour.

Clinical Visit 3 Preparation, Impression, Provisionalisation,

Allocation Impartial third party randomly allocates jaw relation methods to participants and informs laboratory technician of allocation results.

Single unit fixed prosthesis will be fabricated as per allocation results

Clinical Visit 4 Checking and verification of restoration ensuring

1. Proximal contour and contact.
2. Marginal integrity
3. Facial and lingual contours.
4. Surface finish.
5. Color and shade.

Impression prior to occlusal adjustment, Occlusal adjustment, Timing occlusal adjustment procedure, Impression after occlusal adjustment, Cementation.

Conditions

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Dental Occlusion Crowns

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Triple blind (participant, investigator and outcomes assessor), randomized, clinical superiority trial with 1:1:1 allocation ratio.
Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors
All conventional and digital mounting procedures will be performed with all trial participants and the allocation will occur as to which mounting procedure will be utilized in the designing of the crown. Sequence allocation will be performed using a random sequence generated by an impartial third party who will assign an equal number of participants to each mounting condition. This allocation will be shared with the laboratory technician but not the main investigator as he will be performing the outcomes assessments.

Study Groups

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Digitized Mounted Articulator Scan

Conventional articulator facebow mounting will be digitized using extraoral digital 3d scanner and used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Group Type ACTIVE_COMPARATOR

Digitized Mounted Articulator Scan

Intervention Type PROCEDURE

Conventional articulator facebow mounting will be digitized using extraoral digital 3d scanner and used to position the maxillary cast on the virtual articulator. This positioning will be utilized during design of the occlusal surface of the restoration.

Average Positioning on Virtual Bonwill Triangle

Virtual Bonwill triangle will be used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Group Type EXPERIMENTAL

Average Positioning on Virtual Bonwill Triangle

Intervention Type PROCEDURE

Virtual Bonwill triangle will be used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Digital Face Scan

Digital face scan will be used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Group Type EXPERIMENTAL

Digital Face Scan

Intervention Type PROCEDURE

Digital face scan will be used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Interventions

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Digitized Mounted Articulator Scan

Conventional articulator facebow mounting will be digitized using extraoral digital 3d scanner and used to position the maxillary cast on the virtual articulator. This positioning will be utilized during design of the occlusal surface of the restoration.

Intervention Type PROCEDURE

Average Positioning on Virtual Bonwill Triangle

Virtual Bonwill triangle will be used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Intervention Type PROCEDURE

Digital Face Scan

Digital face scan will be used to position the maxillary cast on the virtual articulator.

This positioning will be utilized during design of the occlusal surface of the restoration.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Be aged 21-70 years old, be able to read and sign the informed consent document.
* Psychologically and physically able to withstand conventional dental procedures.
* Participants with molars indicated for full coverage restorations

1. Large carious lesions
2. Teeth restored with large restorations
3. Endodontically treated teeth
* Accept to undergo face scanning and articulator mounting procedures
* Have no active periodontal or pulpal diseases, have teeth with clinically acceptable restorations.
* Able to attend punctually for preplanned visits and evaluation.

Exclusion Criteria

* Participants with active resistant periodontal diseases.
* Participants with poor oral hygiene, high caries risk and uncooperative participants.
* Pregnant women.
* Participants in the growth stage with partially erupted teeth.
* Psychiatric problems or unrealistic expectations.
* Lack of opposing dentition in the area of interest.
* Restored occlusal surface opposing the planned restoration.
* The presence of a removable or fixed orthodontic appliance.
* Signs of bruxism or clenching
Minimum Eligible Age

21 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Aly Ayman Mohamed El-Kady

Assistant Lecturer of fixed prosthodontics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Aly AM El-Kady, MSc

Role: PRINCIPAL_INVESTIGATOR

Fixed Prosthodontics Department, Misr International University

Shereen A Ameen, Prof. Dr.

Role: STUDY_CHAIR

Fixed Prosthodontics Department, Cairo University

Rasha NM Sami, Prof. Dr.

Role: STUDY_DIRECTOR

Fixed Prosthodontics Department, Cairo University

Locations

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Faculty of Dentistry, Cairo University

Giza, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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KADY0001

Identifier Type: -

Identifier Source: org_study_id

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