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The Microbiological Assessment of Deep Carious Lesions After Step-wise Excavation and Diode Laser Cavity Disinfection .

Diode Laser Cavity Disinfection (A Six Month Randomized Clinical Trial).

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03298165
Enrollment
15
Registered
2017-10-02
Start date
2018-02-28
Completion date
2018-06-30
Last updated
2018-01-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Antibacterial Effect of Diode Laser

Brief summary

This study will be conducted to assess antibacterial effect of the diode laser in deep carious cavity after step wise excavation using the bacteriological assessment method.

Detailed description

each patient should have at least two deep carious lesions The first clinical step in all teeth will be the opening of the cavity and the removal of undermined enamel . Caries at the lateral walls of the cavity and at the enamel-dentin junction was completely removed with excavators and/or round carbide burs at low speed. Subsequently, the central cariogenic biomasses and superficial part of the necrotic and demineralized dentin were removed. then excavation continued until the pulp exposure would occur with further excavation; thus, a layer of soft carious dentin was left on the cavity floor adjacent to the pulp wall. A dentine samples will be then collected from the base of the cavity using sterile spoon excavator from the both groups for baseline bacteriological assessment and another sample will be taken after disinfection with diode laser in the intervention group . In the two groups The remaining innermost layer of carious dentin are covered with calcium hydroxide The cavity was then sealed with restorative material (resin modified glass ionomer) after a 6 month period. This time was considered adequate for calcium hydroxide to exert its effect and for the pulp to respond with possible formation of tertiary dentin. The teeth were followed up every month and the integrity of the temporary restoration checked. After this interval of 6 months. After the rubber dam application, the temporary filling is removed samples are collected and the teeth are finally restored

Interventions

DEVICEdiode laser

diode laser has antibacterial effect so can disinfect deep cavity and decrease the count of bacteria present after stepwise excavation

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

outcome assessor the assessor will not be blind about the type of intervention/control assessment methods. however it will not be allowed amongst the examiners to exchange any information throughout the entire study period

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

1. Patients with at least two deep occlusal carious lesion . 2. 18 - 25years. 3. Males or Females. 4. Good oral hygiene. 5. Co-operative patients approving the trial and willing to sign a written consent.

Exclusion criteria

1. Pregnancy. 2. Systemic disease or severe medical complications. 3. Heavy smoking. 4. Xerostomia. 5. Lack of compliance. 6. Evidence of temporomandibular joint disorders.

Design outcomes

Primary

MeasureTime frameDescription
bacteriological count30 minutedentine samples will be taken before and after application of diode laser then bacteriological assessment will be done in the micro-lab

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026