- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05766033
Bracket Failure With a Novel Etchant Paste. A Randomized Clinical Trial (failurerate)
March 17, 2023 updated by: Hussein Qays Aswad, University of Baghdad
Bracket Failure Rate With a Novel Etchant Paste. A Randomized Clinical Trial
To investigate metallic brackets failure rate bonded post enamel conditioning with a novel CaP etchant paste in comparison with those bonded following conventional enamel etching with PA gel over a period of 6 months.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
Acid etching of tooth surfaces to promote the bonding of orthodontic attachments to the enamel has been a routine procedure in orthodontic treatment since the 1960s.
Various types of orthodontic etchants and etching techniques have been introduced in the past five decades.
Michael G Buonocore in revolutionized dentistry with his historical paper: "A simple method of increasing the adhesion of acrylic filling materials to enamel surfaces" depicting the advantage of etching and bonding of acrylic to enamel.
It forever changed the practice of dentistry.
Buonocore and Silverstone led the profession in acid etching and bonding of resin to etched enamel surfaces.
These developments allowed orthodontists to bond brackets reliably and apply forces to move teeth without banding every tooth or having brackets deboned.
Buonocore reported that 85% phosphoric acid etchant significantly increased the adhesion of acrylic resin to enamel.
Since then, a variety of etchants have been used with different concentrations and etching times.
These include hydrofluoric acid, citric acid, hydrochloric acid, maleic acid, nitric acid, and phosphoric acid in a variety of concentrations.
Suggested etching times can vary from 15 to 60 seconds.
The tooth enamel surface is known for its low-energy and hydrophobic properties, with its outermost layer being rich in fluoride.
Enamel etching with phosphoric acid (PA) removes the fluoride-rich layer, dissolves enamel mineral, creates micro- pores, and renders a high-energy and hydrophilic enamel surface to permit wetting by an adhesive; yet at the expense of increased surface porosity, susceptibility to staining, caries, more remnant adhesive and enamel loss.
Fixation of brackets to teeth involves joining of two different solid substrates or adherents through an intervening adhesive layer.
Bracket bases are currently provided with mesh designs that ensure robust mechanical interlocking between the bracket and adhesive, whilst research is ongoing to improve enamel conditioning strategies that can attain clinically successful bond strengths yet maintain an unblemished enamel surface.
Alternative methods to conventional enamel etching with phosphoric acid have been sought aiming at decreasing the bond strength to reduce the incidence of enamel damage.
The use of glass ionomer cements for orthodontic bonding decreased the occurrence of enamel damage, yet at the expense of clinically unacceptable bond strengths.
On the other hand, the use of laser etching and self- etch primers resulted in bracket shear bond strengths comparable to the conventional etch-and-rinse approach, but could not eliminate enamel damage.
In 2019, Ibrahim et al developed a new bioactive orthodontic etchant paste made of calcium-phosphate (CaP), which could alleviate subsurface enamel demineralization in comparison with the traditional phosphoric acid etchant and the pre-clinical viability assessment using in vitro studies showed exemplary advantages.
The new low-pH CaP paste etchant application is a clinically viable bracket bonding method with steps similar to PA application that yielded adequate bond strength with the advantages of minimal adhesive remnants and no enamel chipping or cracking on deboning of the bracket.
Study Type
Interventional
Enrollment (Actual)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alrusafaa
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Baghdad, Alrusafaa, Iraq
- Hussain Qays Aswad
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
12 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria.
- Full permanent dentition including incisors, canines, premolars, and first molars.
- Teeth with sound, non-carious buccal enamel and no pretreatment with chemical agents such as hydrogen peroxide.
- No previous orthodontic treatment with fixed appliances.
Exclusion Criteria:
- Were unable to give informed consent) Had craniofacial anomalies.
- Required orthognathic surgery as part of their treatment.
- Had congenital enamel defects
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Novel etchent paste
|
The maxillary and mandibular incisors, canines, and premolars for each patient will be conditioned using the Novel etchent paste on one side (experimental), while the other side (control) conditioned with a phosphoric acid gel 37% .
Both systems use identical brackets and adhesive system (differ only with regard to the etching system).
Other Names:
|
|
Active Comparator: Phosphoric acid 37%
|
The maxillary and mandibular incisors, canines, and premolars for each patient will be conditioned using the Novel etchent paste on one side (experimental), while the other side (control) conditioned with a phosphoric acid gel 37% .
Both systems use identical brackets and adhesive system (differ only with regard to the etching system).
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bracket failure rate
Time Frame: 6 months
|
Patients with repeated bond failures caused by habits or trauma would be excluded from further analysis.only
counting the number of brackets that broken .
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adhesive remenant index
Time Frame: 6 months
|
Assessment of the amount of remnant adhesive left post bracket failure (for both methods).This index system was developed on the basis of a pilot study of 20 extracted teeth and the criteria were as follows: score 0 = no adhesive left on the tooth; score 1 = less than half of the adhesive left on the tooth; score 2 = more than half of the adhesive left on the tooth; and score 3 = all adhesive left on the tooth with a distinct impression of the bracket mesh.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 2, 2022
Primary Completion (Actual)
February 28, 2023
Study Completion (Anticipated)
October 30, 2023
Study Registration Dates
First Submitted
March 1, 2023
First Submitted That Met QC Criteria
March 1, 2023
First Posted (Actual)
March 13, 2023
Study Record Updates
Last Update Posted (Actual)
March 21, 2023
Last Update Submitted That Met QC Criteria
March 17, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Bracket failure rate
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
till now there is no plan to share it when i found it i will updated it.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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