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A Clinical Trial on the Failure Rates of Metallic and Ceramic Orthodontic Brackets

Primary Purpose

Dental Malocclusion

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Fixed orthodontic treatment with stainless steel brackets
Fixed orthodontic treatment with ceramic brackets
Sponsored by
University of Pavia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Dental Malocclusion focused on measuring metallic brackets, ceramic brackets, bond failures, multibrackets therapy, orthodontic treatment, bonding

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients willing to begin fixed multibracket therapy with metallic or ceramic brackets;
  • full permanent dentition;
  • enamel integrity, absence of traumatic or carious lesions, no pretreatment procedure performed with chemical agents;
  • no previous orthodontic treatment with fixed vestibular appliances.

Exclusion Criteria:

  • patients suffering from systemic diseases;
  • patients taking medications that could alter periodontal conditions (NSAIDS, steroids, etc.);
  • patients with low compliance;
  • patients unable to give informed consent;
  • presence of congenital enamel defects;
  • extractions for orthodontic reasons;
  • oral/orthognathic surgery.

Sites / Locations

  • Unit of Orthodontics and Pediatric Dentistry - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Pediatrics - University of Pavia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Groups MET

Group CER

Arm Description

Patients from this group will undergo orthodontic fixed treatment with stainless steel brackets.

Patients from this group will undergo orthodontic fixed treatment with ceramic brackets.

Outcomes

Primary Outcome Measures

Failure rates of metallic and ceramic brackets.
Each month, failed brackets will be recorded. Per each tooth, failure will be recorded once.

Secondary Outcome Measures

Failure rates of metallic and ceramic brackets per sites and sides.
Failures will be divided in "anterior" for brackets failed on incisors and canines, and "posterior" for premolar brackets. Failure will be recorded per dental arch ("upper" and "lower") and per archwire (.014-in NiTi, .016-in NiTi, .017X0.25-in NiTi, .019X.025-in SS). Per each tooth, failure will be recorded once.
ANB angle
ANB angle will be calculated using the pre-treatment lateral cephalometric radiograph.
Wits Index
Wits Index will be calculated using the pre-treatment lateral cephalometric radiograph.
Skeletal Class
Skeletal Class will be assessed using ANB angle and Wits Index will be calculated using the pre-treatment lateral cephalometric radiograph.
Dento-alveolar discrepancy
Dento-alveolar discrepancy will be calculated using the pre-treatment study models.
Little Index
Little Index will be calculated using the pre-treatment study models.

Full Information

First Posted
November 10, 2021
Last Updated
May 10, 2023
Sponsor
University of Pavia
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1. Study Identification

Unique Protocol Identification Number
NCT05151991
Brief Title
A Clinical Trial on the Failure Rates of Metallic and Ceramic Orthodontic Brackets
Official Title
A 12-months Evaluation of the Failure Rates of Stainless Steel and Ceramic Brackets in Orthodontic Fixed Therapy: a Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
December 9, 2021 (Actual)
Primary Completion Date
May 4, 2023 (Actual)
Study Completion Date
May 8, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pavia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to assess if there are significant differences in the failure rate of stainless steel and ceramic brackets. For this study, patients will be enrolled and divided into two groups, according to the type of brackets (stainless steel or ceramic) used for orthodontic treatment. Failure rates will be recorded every month for 12 months and survival analysis will be performed, together with skeletal and space analysis.
Detailed Description
This clinical trial aims to investigate if there are differences in the failure rates of stainless steel and ceramic orthodontic brackets. Patients willing to start orthodontic fixed therapy and recruited for the study will be asked to sign the informed consent. Parents will sign the consent for underage patients. After that, patients will be divided into two groups: Group MET: stainless steel brackets will be bonded on the vestibular surfaces of teeth. Group CER: ceramic brackets will be bonded on the vestibular surfaces of teeth. The following sequence of archwires will be adopted for the first six months: 0.014-in Niti, .016-in NiTi, 0.017X0.025-in NiTi, 0.019X0.025-in SS. The failure rates of the brackets will be recorded each month for 12 months. Each failed bracket will be recorded once. For each patient, pre-treatment lateral cephalometric radiograph and study models will be used to measure ANB angle, Wits, Skeletal Class, dento-alveolar discrepancy and Little Index at the beginning of the treatment. Bond failures will be recorded together with the archwire engaged at the moment of the failure. Sample size Sample size was calculated with the following assumptions: ability to detect a clinically relevant difference of 4.935% in the failure rates (primary outcome) of the two groups with an alfa = 0.05 and power = 80%. The assumptions were based on findings of a previous study with an expected value of 12.08% for the first group at the end of 12 months of therapy. Therefore, 800 brackets (40 patients) per group were required for the study. Statistical analysis Statistical analysis will be conducted with R software (R version 3.1.3, R Development Core Team, R Foundation for Statistical Computing, Wien, Austria). Fisher exact test will be performed to evaluate the differences between the failure rates of the two groups, between anterior and posterior sites and between upper and lower arches. Kaplan-Meier survival analysis of the bond failures will be performed among the 12 months of the study. Linear regressions will be calculated to assess the effects on bond failure of the skeletal and dental variables collected before the bonding procedure. Significance for all statistical tests will be predetermined at P<0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Malocclusion
Keywords
metallic brackets, ceramic brackets, bond failures, multibrackets therapy, orthodontic treatment, bonding

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Groups MET
Arm Type
Active Comparator
Arm Description
Patients from this group will undergo orthodontic fixed treatment with stainless steel brackets.
Arm Title
Group CER
Arm Type
Active Comparator
Arm Description
Patients from this group will undergo orthodontic fixed treatment with ceramic brackets.
Intervention Type
Other
Intervention Name(s)
Fixed orthodontic treatment with stainless steel brackets
Intervention Description
Orthophosphoric acid 37% acid (Gerhò Etchant gel 37%, Gerhò spa, Terlano, Italy) will be applied for 30 s for the etching of the vestibular surfaces of teeth. The, after rinsing and drying, a thin layer of Transbond XT Light Cure Adhesive Primer (3M Unitek, Monrovia, CA, USA) will be applied and then cured for 10 s with a LED unit. At last, Transbond XT Light Cure Adhesive Paste (3M Unitek) will be applied on the base of stainless steel brackets (Queen Series Low Profile Brackets MBT 0.022", Aestetika, Terni, TR, Italy); brackets will be applied on the vestibular surfaces of teeth with a light pressure and the extra paste will be removed. Curing will be performed with the LED unit at 2 mm distant from the enamel-bracket interface for 40 s, 10 s per each surface (mesial, distal, gingival and occlusal). Then, the following sequence of archwires will be adopted for the first six months: .014-in Niti, .016-in NiTi, .017X.025-in NiTi, .019X.025-in SS (Aestetika, Terni, Italy).
Intervention Type
Other
Intervention Name(s)
Fixed orthodontic treatment with ceramic brackets
Intervention Description
Orthophosphoric acid 37% (acid (Gerhò Etchant gel 37%, Gerhò spa, Terlano, Italy) will be applied for 30 s for the etching of the vestibular surfaces of teeth. The, after rinsing and drying, a thin layer of Transbond XT Light Cure Adhesive Primer (3M Unitek, Monrovia, CA, USA) will be applied and then cured for 10 s with a LED unit. At last, Transbond XT Light Cure Adhesive Paste (3M Unitek) will be applied on the base of ceramic brackets; brackets (Super Clear Series Brackets MBT 0.022", Aestetika, Terni, TR, Italy) will be applied on the vestibular surfaces of teeth with a light pressure and the extra paste is removed. Curing will be performed with the LED unit at 2 mm distant from the enamel-bracket interface for 40 s, 10 s per each surface (mesial, distal, gingival and occlusal). Then, the following sequence of archwires will be adopted for the first six months: .014-in Niti, .016-in NiTi; .017X.025-in NiTi, .019X.025-in SS (Aestetika, Terni, Italy).
Primary Outcome Measure Information:
Title
Failure rates of metallic and ceramic brackets.
Description
Each month, failed brackets will be recorded. Per each tooth, failure will be recorded once.
Time Frame
Among the 12 months of the study.
Secondary Outcome Measure Information:
Title
Failure rates of metallic and ceramic brackets per sites and sides.
Description
Failures will be divided in "anterior" for brackets failed on incisors and canines, and "posterior" for premolar brackets. Failure will be recorded per dental arch ("upper" and "lower") and per archwire (.014-in NiTi, .016-in NiTi, .017X0.25-in NiTi, .019X.025-in SS). Per each tooth, failure will be recorded once.
Time Frame
Among the 12 months of the study.
Title
ANB angle
Description
ANB angle will be calculated using the pre-treatment lateral cephalometric radiograph.
Time Frame
Before the beginning of the orthodontic treatment.
Title
Wits Index
Description
Wits Index will be calculated using the pre-treatment lateral cephalometric radiograph.
Time Frame
Before the beginning of the orthodontic treatment.
Title
Skeletal Class
Description
Skeletal Class will be assessed using ANB angle and Wits Index will be calculated using the pre-treatment lateral cephalometric radiograph.
Time Frame
Before the beginning of the orthodontic treatment.
Title
Dento-alveolar discrepancy
Description
Dento-alveolar discrepancy will be calculated using the pre-treatment study models.
Time Frame
Before the beginning of the orthodontic treatment.
Title
Little Index
Description
Little Index will be calculated using the pre-treatment study models.
Time Frame
Before the beginning of the orthodontic treatment.

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients willing to begin fixed multibracket therapy with metallic or ceramic brackets; full permanent dentition; enamel integrity, absence of traumatic or carious lesions, no pretreatment procedure performed with chemical agents; no previous orthodontic treatment with fixed vestibular appliances. Exclusion Criteria: patients suffering from systemic diseases; patients taking medications that could alter periodontal conditions (NSAIDS, steroids, etc.); patients with low compliance; patients unable to give informed consent; presence of congenital enamel defects; extractions for orthodontic reasons; oral/orthognathic surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Scribante, DDS, PhD
Organizational Affiliation
University of Pavia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Unit of Orthodontics and Pediatric Dentistry - Section of Dentistry - Department of Clinical, Surgical, Diagnostic and Pediatrics - University of Pavia
City
Pavia
State/Province
Lombardy
ZIP/Postal Code
27100
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data will be available upon motivated request to Principal Investigator
Citations:
PubMed Identifier
30972424
Citation
Kirschneck C, Rohn C, Proff P, Reicheneder C. Influence of enamel sealing with a light-cured filled sealant before bracket bonding on the bond failure rate during fixed orthodontic therapy. J Orofac Orthop. 2019 May;80(3):136-143. doi: 10.1007/s00056-019-00174-w. Epub 2019 Apr 10.
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A Clinical Trial on the Failure Rates of Metallic and Ceramic Orthodontic Brackets

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