Effect of Photobiomodulation on ph and Salivary Flow

NCT ID: NCT05413993

Last Updated: 2022-06-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-10

Study Completion Date

2022-05-20

Brief Summary

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Changes in salivary parameters, such as decreased flow, changes in pH and composition, can lead to changes in oral health. Saliva is responsible for the homeostasis of the oral cavity and is therefore directly related to the occurrence of caries, periodontitis, fungal and bacterial infections. These situations compromise the quality of life of the population and for this reason prevention and treatment strategies need to be studied and developed. Photobiomodulation is an alternative that has been increasingly practiced by health professionals. It consists of the application of light to a biological system that is capable of inducing a photochemical process, mainly in the mitochondria, thus stimulating the production of energy in the form of adenosine triphosphate (ATP), which can increase cellular metabolism and produce effects. as analgesia and tissue regeneration. In dentistry, studies using photobiomodulation have shown promise in improving some salivary parameters. This study aimed to compare the action of infrared light on salivary flow and pH, using two application techniques: extraoral (G1) and intra and extraoral (G2), with the application interval between the two techniques being 7 days

Detailed Description

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This is a quasi-experimental clinical study evaluating the flow and salivary pH of healthy adults. The study was carried out with 20 adult patients at the Nove de Julho University. This study aimed to compare the action of infrared light on salivary flow and pH, using two application techniques: extraoral (G1) and intra and extraoral (G2), with the application interval between the two techniques being 7 days. The sample consisted of 20 healthy adults, who participated in both groups, thus being the actual control in the evaluations. Stimulated saliva was collected in both groups before and immediately after light application. In G1, a cluster with 3 spots was used, at a wavelength of 808 nanometers, power of 120 mW, with 24J of energy on the extraoral surface, for 67 seconds, in the region of the parotid gland, region of the submandibular and sublingual glands bilaterally, totaling 4 application regions, with total deposited energy of 96 joules. In G2, the laser was applied for 60 seconds, in 2 intraoral and 2 extraoral points in the region of the parotid glands bilaterally, as well as 1 intraoral and 1 extraoral point in the regions of the submandibular and sublingual glands (totaling 16 points), with a central wavelength of 808 nm; continuous operating mode; power of 100mW; with an aperture diameter of 0.354 cm (with spacer); radiant energy of 6J per point, totaling 96 joules of energy.

Conditions

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Xerostomia

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

QUASI-EXPERIMENTAL CLINICAL TRIAL
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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intra and extraoral application

The laser was applied for 60 seconds, in 2 intraoral points and 2 extraoral points.

Group Type ACTIVE_COMPARATOR

photobiomodulation

Intervention Type RADIATION

Laser application intraorals and extraoral points in the region of the salivary glands bilaterally

extraoral application

The laser was applied only extraoral points

Group Type EXPERIMENTAL

photobiomodulation

Intervention Type RADIATION

Laser application intraorals and extraoral points in the region of the salivary glands bilaterally

Interventions

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photobiomodulation

Laser application intraorals and extraoral points in the region of the salivary glands bilaterally

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* Healthy adults over 18 years of age
* healthy dentition.

Exclusion Criteria

* dental caries
* gingivitis or other alterations in the oral cavity
* who use medication that has the side effect of decreasing the salivary flow,
* who have used an antibiotic or anti-inflammatory within the last 30 days,
* diabetes.
Minimum Eligible Age

10 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Nove de Julho

OTHER

Sponsor Role lead

Responsible Party

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Lara Jansiski Motta

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Nove de Julho Univ

São Paulo, São Paulo, Brazil

Site Status

Countries

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Brazil

Other Identifiers

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PBMSF

Identifier Type: -

Identifier Source: org_study_id

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