Digital Technique to Analyze the Wear of Implants and Natural Tooth as Antagonist.

Sponsor
University of Salamanca (Other)
Overall Status
Completed
CT.gov ID
NCT05842655
Collaborator
(none)
10
1
1
8
1.3

Study Details

Study Description

Brief Summary

The aim of this study was to describe a novel digital technique to analyze the wear of screw-retained implant-supported metal-ceramic dental prostheses and natural tooth as antagonist. Materials and methods: Ten patients were consecutively included to rehabilitate partial edentulism by dental implants. Both the screw-retained implant-supported metal-ceramic dental prostheses and the natural tooth as antagonist were submitted to a digital impression through an intraoral scan to generate a Standard Tessellation Language digital file preoperatively (STL1), at 3 months (STL2), and 6 months (STL3) follow-up. Afterwards, an alignment procedure of the digital files (STL1-STL3) was performed on a reverse engineering morphometric software and volume changes at the screw-retained implant-supported metal-ceramic dental prostheses and the natural tooth as antagonist were analyzed using Student's t-test. Moreover, Gage R&R statistical analysis was conducted to analyze the repeatability and reproducibility of the digital technique.

Condition or Disease Intervention/Treatment Phase
  • Procedure: The wear of screw-retained implant-supported metal-ceramic dental prostheses and natural tooth
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Digital Technique to Analyze the Wear of Screw-Retained Implant-Supported Metal-Ceramic Dental Prostheses and Natural Tooth as Antagonist. A Pilot Study
Actual Study Start Date :
Jan 1, 2022
Actual Primary Completion Date :
Mar 1, 2022
Actual Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients thats were chosen in order to rehabilitate partial edentulism by dental implants.

Procedure: The wear of screw-retained implant-supported metal-ceramic dental prostheses and natural tooth
A novel digital technique to analyze the wear of screw-retained implant-supported metal-ceramic dental prostheses and natural tooth as antagonist

Outcome Measures

Primary Outcome Measures

  1. Wear volume (µm3) of the screw-retained implant-supported metal-ceramic dental prostheses [3 months follow-up appointment]

    Wear volume (µm3) of the screw-retained implant-supported metal-ceramic dental prostheses at 3 months follow-up appointment

  2. Wear volume (µm3) of the screw-retained implant-supported metal-ceramic dental prostheses [6 months follow-up appointment]

    Wear volume (µm3) of the screw-retained implant-supported metal-ceramic dental prostheses at 6 months follow-up appointment

  3. Wear volume (µm3) of the natural tooth as antagonist [3 months follow-up appointment]

    Wear volume (µm3) of the natural tooth as antagonist at 3 months follow-up appointment

  4. Wear volume (µm3) of the natural tooth as antagonist [6 months follow-up appointment]

    Wear volume (µm3) of the natural tooth as antagonist at 6 months follow-up appointment

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • in good health, who presented partial edentulism in the posterior upper maxilla, were consecutively included to rehabilitate partial edentulism by dental implants
Exclusion Criteria:
  • all those who do not meet the inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Salamanca Salamanca Spain 37008

Sponsors and Collaborators

  • University of Salamanca

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
JAVIER MONTERO, Principal Investigator, University of Salamanca
ClinicalTrials.gov Identifier:
NCT05842655
Other Study ID Numbers:
  • USAL 2022-AZM
First Posted:
May 6, 2023
Last Update Posted:
May 6, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by JAVIER MONTERO, Principal Investigator, University of Salamanca
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2023