Microbial and Periodontal Changes Associated With Conventional Versus Self Ligating Brackets

May 5, 2015 updated by: Esam Al-hendi, Al-Azhar University

Faculty of Dental Medicine, Boys, Cairo Al-Azhar University

Microbial and periodontal changes associated with conventional versus self ligating brackets.

The aim of this study will be to compare microbial and periodontal changes associated with conventional versus self ligating brackets.

Study Overview

Detailed Description

Microbial and periodontal changes associated with conventional versus self ligating brackets.

Protocol submitted in partial fulfillment for the requirements of Master Degree in Orthodontics

Accumulation of biofilm on the tooth surfaces is associated with increased levels of oral streptococcus mutans and lactobacilli, which have been proved to be responsible for the onset of enamel demineralization and periodontal disease.

It has been shown that fixed appliance provides large number of retentive areas for plaque accumulation and impedes oral hygiene.

Three methods are currently used to connect the arch wire to the brackets, which are : ligation with stainless steel ligatures , using elastomeric ligatures, and the self-ligating brackets. , Each of these method has it's advantages and disadvantages, concerning the biofilm retention and the level of microorganisms. , Orthodontic treatment with conventional brackets my presents some periodontal changes caused by difficulty in oral hygiene maintenance, greater accumulation and qualitative alteration of plaque. Thus, in order to control oral hygiene and plaque level during fixed appliance therapy, manufacturers introduced self-ligating brackets (SLBs) which have been claimed to provide better oral hygiene and less plaque accumulation, because of fewer retentive sites for microbial colonization; without the need for stainless steel and elastomeric ligature. Clinically, the side effects of fixed orthodontic treatment, such as the qualitative bacterial shift, are manifested as plaque associated gingivitis, an increase in pocket probing depth (PPD), and bleeding on probing.

Fewer studies have compared conventional and self-ligating brackets in relation to oral hygiene, microbial count and periodontal indices. Therefore, the present study will be conducted to evaluate and compare microbial and periodontal changes with conventional and self ligating brackets.

The aim of this study will be to compare microbial and periodontal changes associated with conventional versus self ligating brackets.

Subjects and method

Study design:

Randomized controlled clinical trial

Study setting and population:

The sample of this study will be consisted of forty five patients selected from Outpatient Clinic, Orthodontic Department, Faculty of Dental Medicine, Boys, Cairo, Al-Azhar University.

Interventions:

The patients will be divided randomly into three groups and will be treated separately as follows:

  • Group I: will be treated using conventional stainless steel orthodontic brackets ligated with stainless steel ligature.
  • Group II: will be treated using passive self-ligating stainless steel orthodontic brackets.
  • Group III: will be treated by active self-ligating stainless steel orthodontic brackets.

Records:

For all patients the following records will be taken before and after treatment:

  1. Standardized Orthodontic study cast.
  2. Standardized intra oral and extra oral photographs.
  3. Standardized panoramic radiograph.
  4. Standardized lateral cephalometric radiograph.

Observations:

• Periodontal parameters: The following clinical parameters will be recorded at baseline before treatment and at monthly interval for 6 months after bonding;

  1. Pocket probing depth .
  2. Plaque index (Silness and Loe) .
  3. The presence or absence of bleeding on probing .

    • Microbial parameters:

Plaque sample will be taken at base line and at monthly interval for six months after bonding. The sample will be taken from the maxillary left canine, second premolar and the right central incisor and the mandibular right canine, second premolar and the left central incisor.

Plaque sample will be send to laboratory for isolation of streptococcus mutans and lactobacilli. The isolated strains will be cultured and counted.

Ethical consideration:

All patients will clearly understand the purpose of the study and give their consent by signing an informed consent (attached copy of the consent form).

Patient's instructions:

Instructions form (a copy attached) will be signed by all patients and their parents before commencing the study.

Data management and analysis:BN All the obtained results will be gathered and statistically analyzed using Statistical Package for Social Sciences (SPSS, version 16, Inc., Chicago, Ill).

Study Type

Interventional

Enrollment (Anticipated)

45

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

      • Cairo, Egypt
        • Recruiting
        • Faculty of Dentistry
        • Contact:

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

14 years to 18 years (ADULT, CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

All patients should satisfy the following criteria:

  1. Age ranged between 14-18 years.
  2. All permanent teeth erupted (excluding third molars).
  3. Angle Class I with normal facial proportion.
  4. Moderate crowding (from 4 to 6 mm) or irregularity index greater than 4.
  5. All cases require treatment with fixed appliance with non extraction approach.
  6. Good oral and general health.
  7. No previous or current periodontal diseases.
  8. No systemic disease or medication that may interfere with orthodontic teeth movement.
  9. No history of trauma, bruxism or parafunction.
  10. No previous orthodontic treatment.

Exclusion Criteria:

  1. Abnormal anteroposterior relationship or steep mandibular plane.
  2. Crowding more than 6 mm.
  3. Poor oral hygiene or periodontal affection.
  4. Uncooperative patients.
  5. Smoker patients.
  6. Pregnant females.

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: HEALTH_SERVICES_RESEARCH
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Group I:

will be treated using conventional stainless steel orthodontic brackets ligated with stainless steel ligature. Oromco - USA.

.

Other Names:
  • conb
Experimental: Group II
: will be treated using passive self-ligating stainless steel orthodontic brackets Oromco - USA.
Other Names:
  • pasb
Experimental: Group III:
will be treated by active self-ligating stainless steel orthodontic brackets Oromco - USA .
Other Names:
  • actb

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pocket depth
Time Frame: every month for six months
Pocket depth measured by a Williams periodontal probe at baseline before treatment and at monthly interval for 6 months after bonding.
every month for six months
plaque accumulation
Time Frame: every month for 6 months after bonding.
plaque accumulation will be assess using Silness and Loe index
every month for 6 months after bonding.
Gingival bleeding
Time Frame: every month for 6 months after bonding.
Gingival bleeding will be evaluated by the presence or absence of bleeding on probing
every month for 6 months after bonding.
Composite measure of Microbial parameters
Time Frame: every month for 6 months after bonding.
Plaque sample will be taken at base line and at monthly interval for six months after bonding Plaque sample will be send to laboratory for isolation of streptococcus mutans and lactobacilli. The isolated strains will be cultured and counted
every month for 6 months after bonding.

Collaborators and Investigators

This is where you will find people and organizations involved with this 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

March 1, 2015

Primary Completion (Anticipated)

April 1, 2016

Study Registration Dates

First Submitted

April 19, 2015

First Submitted That Met QC Criteria

May 5, 2015

First Posted (Estimate)

May 6, 2015

Study Record Updates

Last Update Posted (Estimate)

May 6, 2015

Last Update Submitted That Met QC Criteria

May 5, 2015

Last Verified

February 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 005OR.

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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