Survival of Hybrid Laminate Veneers Using Two Different Tooth Preparation Techniques:Randomized Clinical Trial
Primary Purpose
Discoloration, Tooth, Malformed Tooth, Diastema
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
traditional technique of tooth preparation
aesthetic preevaluative temporary technique for tooth preparation
Sponsored by
About this trial
This is an interventional treatment trial for Discoloration, Tooth focused on measuring veneers, hybrid ceramics, CAD/CAM, tooth preparation techniques, USPHS criteria
Eligibility Criteria
Inclusion Criteria:
Patient-related criteria:
- Patients consulting the outpatient clinic of the department of Fixed Prosthodontics, Faculty of Dentistry, Cairo University.
- Able to tolerate necessary restorative procedures.
- Provide written consent.
- Accepts the one year follow-up period.
Tooth related criteria:
- Malaligned and malformed teeth in the aesthetics zone
- Multiple spacing
- Diastema
- Slightly and moderately discolored teeth
- Good oral hygiene
Exclusion Criteria:
Patient-related criteria:
- Medically compromised patients, as they would not be able to attend multiple appointments or might require special management.
- Uncooperative patients, who would not abide by the instructions or attend the appointments.
Tooth related criteria:
- Deciduous teeth; as the study was targeting only permanent teeth.
- Teeth with previous restorations, which might add another variable to the study (type of old restorative material, extent of recurrent caries). This could also affect the bond of laminate veneers to tooth structure.
- Patients with parafunctional habits, large restorations, or excessive tooth wear.
- Initially, scaling and polishing was performed. Patients were instructed on improving their oral hygiene and maintaining effective plaque control. However, if their gingival health did not improve, they were excluded from the study.
Sites / Locations
- Yara Attia
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Traditional technique for tooth preparation.
Aesthetic preevaluative temporary technique
Arm Description
Tooth preparation performed directly on the tooth structure
Aesthetic pre-evaluative temporary (APT) was fabricated according the planned wax-up. Once the APT was approved both aesthetically and functionally, tooth preparation was performed through the APT.
Outcomes
Primary Outcome Measures
Survival of laminate veneers using modified USPHS
Patients were called back after 1 week as the baseline to assess the veneer restorations. Assessment was carried out by an experienced observer blinded to the assigned study group for each patient. Laminate veneers were examined at baseline, after 3, 6 and 12 months according to the modified United States Public Health Service (USPHS) criteriae and the USPHS scores of Alfa, Bravo and Charlie were used for rating . Patients were also questioned about possible post-operative complaints. Digital photographs were made after placement of the veneers and during follow-up sessions.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04515069
Brief Title
Survival of Hybrid Laminate Veneers Using Two Different Tooth Preparation Techniques:Randomized Clinical Trial
Official Title
Survival of a Recent Polymer- Infiltrated Ceramic Network Laminate Veneer Material Using Aesthetic Preevaluative Temporary (APT) Technique Versus Traditional Technique in the Aesthetic Zone:Randomized Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
April 13, 2017 (Actual)
Primary Completion Date
March 20, 2019 (Actual)
Study Completion Date
May 5, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The aim of this study was to evaluate the survival of laminate veneers constructed using a recent polymer-infiltrated ceramic network material following the aesthetic pre-evaluative temporary (APT) technique of tooth preparation in comparison to traditional technique.
Detailed Description
Six recruited patients (4 females, 2 males; ranging from: 20-30 years old and with mean age 24.6 years), who needed indirect laminate veneer restorations were included in this study. Patients were selected from the outpatient clinic of the Department of Fixed Prosthodontics,Faculty of Dentistry, Cairo University The participants received a total of 54 laminate veneers between April 2017 and February 2018. Written informed consent was acquired from all participating patients. Randomization was done using a computer generated 2 column list by the aid of Random.org in a 1:1 ratio. Allocation concealment was achieved using numbered cards in opaque sealed envelopes. Aluminium foil was placed inside the envelope to render the envelope impermeable to intense light. These envelopes were placed in a box and each participant was allowed to grasp one envelop the day of operation. Allocation concealment was performed by an investigator with no clinical involvement in the trial. This study is a single blinded study as the assessor was blinded to the assigned study groups. Blinding of the participants was not applicable as one of the techniques required extra visits. Blinding of the operator was not applicable as one clinician performed the tooth preparation in both techniques.A total of 54 laminate veneers were divided into two equal groups (n=27) according to the technique of tooth preparation: group T: traditional technique and group A: aesthetic pre-evaluative temporary technique. VITA ENAMIC material was used for CAD/CAM construction of laminate veneers. Cementation was performed using a light cured resin cement. The laminate veneers were evaluated at baseline, after 3, 6 and 12 months according to the modified United States Public Health Service (USPHS) criteriea. The data was collected, tabulated and statistically analyzed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Discoloration, Tooth, Malformed Tooth, Diastema
Keywords
veneers, hybrid ceramics, CAD/CAM, tooth preparation techniques, USPHS criteria
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Randomization was done using a computer generated 2 column list by the aid of Random.org in a 1:1 ratio. Allocation concealment was achieved using numbered cards in opaque sealed envelopes. Aluminium foil was placed inside the envelope to render the envelope impermeable to intense light. These envelopes were placed in a box and each participant was allowed to grasp one envelop the day of operation. Allocation concealment was performed by an investigator with no clinical involvement in the trial. This study is a single blinded study as the assessor was blinded to the assigned study groups. Blinding of the participants was not applicable as one of the techniques required extra visits. Blinding of the operator was not applicable as one clinician performed the tooth preparation in both techniques.
Allocation
Randomized
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Traditional technique for tooth preparation.
Arm Type
Active Comparator
Arm Description
Tooth preparation performed directly on the tooth structure
Arm Title
Aesthetic preevaluative temporary technique
Arm Type
Active Comparator
Arm Description
Aesthetic pre-evaluative temporary (APT) was fabricated according the planned wax-up. Once the APT was approved both aesthetically and functionally, tooth preparation was performed through the APT.
Intervention Type
Procedure
Intervention Name(s)
traditional technique of tooth preparation
Other Intervention Name(s)
Group T
Intervention Description
Depth cutter wheels of predetermined depths (Komet, Germany) were used to perform the preparation directly on the tooth structure.
Depth cuts were performed on the labial surface using depth cutter wheels (Komet, Germany) with radius of 0.3 mm and 0.5 mm which is directly related to the thickness of the laminate veneers in the cervical and incisal one thirds respectively. Then islands of tooth structure between depth orientation grooves were removed.
Proximal reduction:
The interproximal reduction was completed just labial to the contact areas using a round end tapered diamond stone (Mani, Japan), and polishing was performed using polishing strips (Sof-Lex, 3M ESPE, Seefeld, Germany).
Incisal reduction:
Vertical depth grooves were created. Then, the round end tapered diamond stone (Mani, Japan)was used to create 1.5 mm incisal butt joint preparation.
Then, finishing and polishing of tooth preparation was performed.
Intervention Type
Procedure
Intervention Name(s)
aesthetic preevaluative temporary technique for tooth preparation
Other Intervention Name(s)
Group A
Intervention Description
The data obtained from digital smile design was used for construction of the diagnostic wax-up. The wax-up was then be transferred to the mouth using a silicone index, creating the aesthetic pre-evaluative temporary (APT). The APT was tested esthetically and functionally. Once approved by the operator and the patient, tooth preparation was performed through the APT. Depth cuts were performed similar to those performed in the traditional preparation with the difference of being prepared on the aesthetic pre-evaluative temporary instead of directly on the dental structure. Using tapered stone with round end (Mani, Japan), islands of tooth structure between depth orientation grooves were removed.
Proximal reduction, Incisal reduction Finishing and polishing of tooth preparation were carried out using the same technique as in the Group T with the difference of being performed through the APT, resulting in minimal tooth preparation
Primary Outcome Measure Information:
Title
Survival of laminate veneers using modified USPHS
Description
Patients were called back after 1 week as the baseline to assess the veneer restorations. Assessment was carried out by an experienced observer blinded to the assigned study group for each patient. Laminate veneers were examined at baseline, after 3, 6 and 12 months according to the modified United States Public Health Service (USPHS) criteriae and the USPHS scores of Alfa, Bravo and Charlie were used for rating . Patients were also questioned about possible post-operative complaints. Digital photographs were made after placement of the veneers and during follow-up sessions.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
44 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patient-related criteria:
Patients consulting the outpatient clinic of the department of Fixed Prosthodontics, Faculty of Dentistry, Cairo University.
Able to tolerate necessary restorative procedures.
Provide written consent.
Accepts the one year follow-up period.
Tooth related criteria:
Malaligned and malformed teeth in the aesthetics zone
Multiple spacing
Diastema
Slightly and moderately discolored teeth
Good oral hygiene
Exclusion Criteria:
Patient-related criteria:
Medically compromised patients, as they would not be able to attend multiple appointments or might require special management.
Uncooperative patients, who would not abide by the instructions or attend the appointments.
Tooth related criteria:
Deciduous teeth; as the study was targeting only permanent teeth.
Teeth with previous restorations, which might add another variable to the study (type of old restorative material, extent of recurrent caries). This could also affect the bond of laminate veneers to tooth structure.
Patients with parafunctional habits, large restorations, or excessive tooth wear.
Initially, scaling and polishing was performed. Patients were instructed on improving their oral hygiene and maintaining effective plaque control. However, if their gingival health did not improve, they were excluded from the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hanaa Zaghloul, PhD
Organizational Affiliation
Professor of Fixed Prosthodontics, Misr International University
Official's Role
Study Director
Facility Information:
Facility Name
Yara Attia
City
Cairo
ZIP/Postal Code
11728
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Clinical Study Report
IPD Sharing Time Frame
starting 6 months after publication
IPD Sharing Access Criteria
Data will be available for students and researchers
Learn more about this trial
Survival of Hybrid Laminate Veneers Using Two Different Tooth Preparation Techniques:Randomized Clinical Trial
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