Er:YAG Laser Treatment of Moderate Chronic Periodontitis

NCT ID: NCT05217823

Last Updated: 2022-02-23

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

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-01-31

Study Completion Date

2014-02-28

Brief Summary

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The Er:YAG laser possesses specific characteristics allowing to be used in non-surgical periodontal treatment. The aim of the resent study was to evaluate the long-term clinical effectiveness of Er:YAG laser monotherapy in the treatment of moderate chronic periodontitis and to compare it with conventional hand instrumentation.

MATERIALS AND METHODS: 451 teeth (1,099 periodontal pockets) from 30 patients with moderate chronic periodontitis (initial probing pocket depth 4 to 6 mm) were allocated for subgingival scaling and root planing in two groups - hand instrumentation (control) and Er:YAG laser instrumentation with 100mJ/15Hz (test). Using a computerized periodontal probe, patients were examined for probing pocket depth (PPD), gingival recession (GR), clinical attachment level (CAL), bleeding on probing (BOP), plaque presence (FMPS) at baseline, one, three, six and 12 months after instrumentation.

Detailed Description

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Conditions

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Chronic Periodontitis, Generalized, Moderate

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Er:YAG laser

Teeth treated with Er:YAG laser

Group Type EXPERIMENTAL

Er:YAG laser

Intervention Type DEVICE

Hand instruments

Teeth treated with Gracey curettes

Group Type ACTIVE_COMPARATOR

hand instruments

Intervention Type OTHER

Interventions

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Er:YAG laser

Intervention Type DEVICE

hand instruments

Intervention Type OTHER

Other Intervention Names

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Er:YAG laser, LiteTouch, Light Instruments, Israel Gracey curettes

Eligibility Criteria

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Inclusion Criteria

* at least two teeth per quadrant with PPD between 3,6 mm and 6,4 mm;
* loss of clinical attachment up to 4 mm
* bleeding on probing

Exclusion Criteria

* periodontal treatment in the last 12 months;
* systemic diseases;
* systemic medication
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Plovdiv Medical University

OTHER

Sponsor Role lead

Responsible Party

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Blagovesta Yaneva

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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Er:YAG - chronic periodontitis

Identifier Type: -

Identifier Source: org_study_id

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