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Comparison of Laser and Chlorhexidine Gel and Treatment of gingival disease.

Not Applicable
Conditions
Chronic Periodontitis.
Chronic periodontitis
Registration Number
IRCT2012070210155N1
Lead Sponsor
Dental and Periodontal Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
24
Inclusion Criteria

The participants with the following inclusion criteria included in the study: modera-to-severe chronic periodontitis, no active periodontal treatment during the past 6 months, presence of at least one site per quadrant exhibiting pocket depth of =4 mm with bleeding on probing.
The exclusion criteria were: use of antibiotics for the past 6 months; previous periodontal surgery for the past 9 months,smoker persons; pregnant or lactating women; subjects with any systemic condition which might influence the course of periodontal disease or treatment (HIV/AIDS, uncontrolled diabetes); any active malignancy of any sort.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Probing depth. Timepoint: At baseline, one month and three month after baseline. Method of measurement: In millimetre by periodontal probe.
Secondary Outcome Measures
NameTimeMethod
Quantitative levels of Porphyromonas Gingivalis. Timepoint: baseline,3 month later. Method of measurement: quantitative measurement by real-time polymerase chain reaction.;Clinical attachment level (CAL). Timepoint: Baseline, 1 month and 3 month after baseline. Method of measurement: In millimetre by periodontal probe.;Gingival recession (REC). Timepoint: Baseline, 1 month and 3 month later. Method of measurement: In millimetre by periodontal probe.;Bleeding on probing (BOP). Timepoint: Baseline, 1 month and 3 month after baseline. Method of measurement: In millimetre by periodontal probe.
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