Evaluation of Gingival Health Parameters in Hybrid CAD / CAM Crowns Produced After Different Retraction Processes

Sponsor
Yuzuncu Yıl University (Other)
Overall Status
Completed
CT.gov ID
NCT03816930
Collaborator
(none)
52
1
3
15
3.5

Study Details

Study Description

Brief Summary

Clinically, the gingival retraction dentistry itself has found wide uses. It has achieved the use of subgingival and gingival crowns in fixed prostheses, cervical abrasion in restorative dentistry, management of root caries and root sensitivity, and recently in the use of appropriate measurements to improve the marginal fit of implant prostheses.There are three different retraction procedures described in the literature: mechanical, mechanical-chemical (chemically impregnated cords or matrix in injectable form) and surgery (electrosurgical, laser, cauterization, etc.)The mechanical method of retraction cords is not always suitable for patients' existing pocket depth, the necessity of using different combinations in shallow or deep pockets, the potential for limited bleeding control in chemically impregnated cords and the toxicity values in those who interact with chemical have led researchers to search for alternative methods. Especially inflammed gingiva is very sensitive to mechanical and chemical trauma. Studies have reported that gingival inflammation, pain, pocket formation, gingival withdrawal, increased bleeding and wound contamination occurred following retraction cord application. However, it is a known fact that the impression material is distorted or the accuracy of the measurement is decreased with the measurements taken without retraction. Nowadays, CAD / CAM (computer-aided design / computer-aided manufacturing) devices, which are designed to overcome these problems and eliminate the errors related to the measurement material, are the first step to be taken with a clear measure.Gingival retraction is recommended to improve the success of scanners in all restorations performed at the gingival or subgingival endpoint. Therefore, in our study, crown restorations will be produced from hybrid blocks by means of CAD / CAM device in order to evaluate the interaction of gingival health with hybrid blocks and to provide the latest technology and standardization.

Condition or Disease Intervention/Treatment Phase
  • Procedure: mechanical cord usage
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
52 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Evaluation of Gingival Health Parameters in Hybrid CAD / CAM Crowns Produced After Different Retraction Processes
Actual Study Start Date :
Jan 17, 2019
Actual Primary Completion Date :
Jan 17, 2020
Actual Study Completion Date :
Apr 17, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Mechanical cord usage

Mechanical retraction

Procedure: mechanical cord usage
Due to the retraction procedures, same preparation conditions will be obtained.
Other Names:
  • Chemical contained retraction usage
  • MZ-6 laser tip used throughing
  • Active Comparator: Chemical contained retraction usage

    Chemical retraction

    Procedure: mechanical cord usage
    Due to the retraction procedures, same preparation conditions will be obtained.
    Other Names:
  • Chemical contained retraction usage
  • MZ-6 laser tip used throughing
  • Active Comparator: MZ-6 laser tip used throughing

    Laser retraction

    Procedure: mechanical cord usage
    Due to the retraction procedures, same preparation conditions will be obtained.
    Other Names:
  • Chemical contained retraction usage
  • MZ-6 laser tip used throughing
  • Outcome Measures

    Primary Outcome Measures

    1. Retraction methods or procedures effects on gingival health [3-12 months]

      Probing depth is one of the criteria that shows the gingival health. In each control sessions same researcher measure the probing depth as mm via a periodontal probe.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 60 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Being systemically healthy

    • To indicate crown restoration in mandibular molar teeth

    • To be vital to the preparation of the crown of the teeth

    Exclusion Criteria:
    • Systemically unhealthy individuals

    • Endodontic treatment of mandibular molar teeth

    • Mandibular molar female individuals drawn for various reasons

    • Pregnant women

    • Periodontally unhealthy individuals

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beyza Ünalan Değirmenci Van Turkey 65080

    Sponsors and Collaborators

    • Yuzuncu Yıl University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Beyza Ünalan Değirmenci, Assistant Professor, Yuzuncu Yıl University
    ClinicalTrials.gov Identifier:
    NCT03816930
    Other Study ID Numbers:
    • 05
    First Posted:
    Jan 25, 2019
    Last Update Posted:
    Apr 22, 2021
    Last Verified:
    Apr 1, 2021
    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 Beyza Ünalan Değirmenci, Assistant Professor, Yuzuncu Yıl University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 22, 2021