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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05217823
Other study ID # Er:YAG - chronic periodontitis
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2012
Est. completion date February 2014

Study information

Verified date February 2022
Source Plovdiv Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date February 2014
Est. primary completion date February 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Er:YAG laser

Other:
hand instruments


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Plovdiv Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary Probing pocket depth Change in PPD (measured as a distance between the gingival margin and the depth of the pocket) using computerised periodontal probe 1 year
Secondary Gingival recession Change in GR (measured as a distance between the gingival margin and the cement-enamel junction) using computerised periodontal probe 1 year
Secondary Clinical attachment level Change of CAL (measured as a distance between the cement-enamel junction and the depth of the pocket) using computerised periodontal probe 1 year
Secondary Bleeding on probing Change in BoP 1 year
Secondary Plaque level Change of Plaque index 1 year
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