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Er:YAG Laser Effects on Microbial Population in Conservative Dentistry

U

University Of Perugia

Status

Completed

Conditions

Dental Caries
Microbial Colonization

Treatments

Device: Er:YAG Laser

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to verify the quantitative and qualitative effect of Erbium dental laser therapy on microbial populations in carious lesions and to compare the laser therapy with traditional conservative therapies.

Full description

Patients will be assessed and selected at the University Odontostomatology Clinic (COU) in Perugia; patients are considered eligible for enrolment if they are at least 18 years old and have a carious lesion on permanent teeth, cavitated and non-destructive, deepening to the middle third of the dentine and no further. The patients will be randomly assigned to two groups as follows: group A, control group, which includes treatment with traditional therapy; group B, intervention group, which includes treatment with Er:YAG laser therapy. For each patient, two salivary swabs will be taken on the cavity dentine of the carious lesion: one before and one after the treatments.

Enrollment

33 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult patients of both sexes with at least 18 years of age and one cavitated non-destructive carious occlusal lesion of a permanent teeth, that deepens up to the middle third of the dentin and not beyond, confirmed by radiographic exam and without pulp involvement.

Exclusion criteria

  • patients that refused to sign the informed consent document;
  • children or individuals with less than 18 years;
  • pregnant subjects;
  • patients with syndromes or chronic systemic diseases;
  • patients who had used antibiotics within the previous three months or under pharmacological treatments;
  • patients with painful symptoms consistent with irreversible pulpitis or mobility and destructive carious lesions extending beyond the middle third of the dentin;
  • teeth with exposure of the dental pulp or periodontitis;
  • patients with caries on deciduous teeth;
  • patients with no cooperation during the radiographical exam and/or treatments.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

33 participants in 2 patient groups

Er:YAG laser therapy group
Active Comparator group
Description:
The removal of caries was performed with Er:YAG laser (Doctor Smile, Lambda SRL,Italy) with BOOST handpiece to cut the enamel and open the cavity, and 90° handpiece to remove the carious dentin with tips of 800 µ in diameter and 8 mm or 12 mm in length, in relation to the depth and distance of the lesion.
Treatment:
Device: Er:YAG Laser
Traditional therapy group
No Intervention group
Description:
The removal of caries was performed with manual and rotating instruments, such as dentin spoon (ASA Dental S.p.a.), turbine (NSK Dental Italy S.r.l.) with diamond burs (Kerr Dental Italia S.r.l.) to cut the enamel and open the cavity and drill handpiece (KaVo Dental Italia S.r.l.) with tungsten carbide burs (Kerr Dental Italia S.r.l.) to remove the infected dentin.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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