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

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

Status

Completed

Conditions

Plaque

Treatments

Device: Airpolishing and ultrasonic debridement

Diagnostic Test: Plaque Disclosing Agent

Study type

Interventional

Funder types

Other

Identifiers

NCT05428189

ORTOPLAK

Details and patient eligibility

About

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).

Full description

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).

Enrollment

32 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

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.