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Completed

NCT Number: NCT05428189

Efficacy of the Disclosing Plaque Agent as a Guide to Remove the Oral Biofilm in Orthodontic Patients.

It is more difficult to perform excellent professional oral hygiene in patients wearing orthodontic appliances.

The hypothesis of the present randomized controlled trial is that the application of plaque disclosing agent allows better biofilm removal.

To test this hypothesis, the patients, upon initial evaluation, will be divided in 2 study groups:

* CONTROL GROUP will receive professional oral hygiene without disclosing agent * TEST GROUP will receive professional oral hygiene guided by plaque disclosing agent

At the end of the professional oral hygiene session, the disclosing agent is re-applied in all patients and the percentage of residual plaque area is calculated though image software analysis (ImageJ).

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Magda

Brescia, Lombardy, 25123, Italy

About this study

Oral biofilm is not always visible, so its complete removal can be challenging. Applying a plaque disclosing agent before the therapy might serve as a guide to better remove biofilm. Thanks to this tool, the clinicians can clearly see where the plaque is, so its removal can be more thorough.

In orthodontic patients, it is even more difficult to remove biofilm and plaque, as the fixed appliances pose an obstacle. The hypothesis is that using a plaque disclosing agent as a guide to the operator, better removal of the biofilm can be achieved.

The study will be performed to assess the efficacy of disclosing plaque agent as a guide to remove biofilm and plaque in orthodontic patients during professional oral hygiene, performed with air-polishing with erythritol powder and a ultrasonic device.

TRIAL DESIGN: Monocetric, pragmatic, single blinded, randomized clinical trial (RCT) of parallel design.The trial will have one-year duration.

STUDY POPULATION: Orthodontic patients with plaque index above the 25% and without periodontal disease.

PRIMARY OUTCOME: the percentage of area in which the disclosing plaque agent is present after the treatment (RPA: Residual Plaque Area).

RPA: residual plaque area: percentage of area with residual plaque coloured by plaque disclosing agent. This will be analysed and calculated with a image analysis software (ImageJ).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed Informed Consent Form;
  • Male and female subjects, aged 18-75 years, inclusive;
  • Presence of orthodontic appliances;
  • Good general health (free of systemic diseases such as diabetes, HIV infection or genetic disorder, ongoing malignant disease of any type that could influence the outcome of the treatment and might interfere with the evaluation of the study objectives);
  • Generalized gingivitis;
  • Plaque index (PI) above 25%;
  • Availability for session of the study for an assigned subject;
  • Presence of all inferior and superior anterior teeth from canine to canine;
  • Smoking less than 10 cigarettes a day.

Exclusion criteria

  • Chronic obstructive pulmonary disease and asthma;
  • Patients with periodontally disease defined as presence of PPD >= 4mm and /or PAL of >=3m;
  • Splinted teeth;
  • Presence of prosthesis;
  • Tumors or significant pathology of the soft or hard tissues of the oral cavity;
  • Current radiotherapy or chemotherapy;
  • Pregnant or lactating women;
  • History of allergy to Erythritol;
  • History of adverse reactions to lactose or fermented milk products;
  • Restorations on the teeth to be treated which may interfere with treatment administration and/or scoring procedures, at the discretion of the examiner;
  • Not willing to follow the agreed protocol.

Treatment and study plan

Plaque Disclosing Agent

Diagnostic Test

A plaque disclosing agent is applied on teeth to detect plaque. Air-polishing will be used as main instrument for biofilm and stains removal, followed by ultrasonic scaling.

Airpolishing and ultrasonic debridement

Device

Air-polishing will be used as main instrument for biofilm and stains removal, followed by ultrasonic scaling.

Primary outcomes

  1. Residual Plaque Area (RPA)

    Time frame: At the end of the treatment session

    The percentage of area in which plaque is still present, as revealed by re-application of plaque disclosing agent, in both groups at the end of the treatment session

Sponsors and collaborators

Lead sponsor

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

Other

Registry information

Official study title

Efficacy of the Disclosing Plaque Agent as a Guide to Remove the Oral Biofilm in Orthodontic Patients: a Randomised Controlled Trial Study

Acronym: ORTOPLAK

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Jun 22, 2022
Registry last updated
Jun 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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