Evaluation of Clinical Periodontal Parameters After Scaling and Root planning with Er:YAG Laser Compared to Ultrasonic Instruments for treatment of Moderate Chronic Periodontitis
- Conditions
- Moderate chronic periodontitis.Chronic periodontitis
- Registration Number
- IRCT201402164877N18
- Lead Sponsor
- Vice of Research, School of Dentistry, Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
moderate chronic periodontitis disease; age over 18 years; lack of systemic disease that can affect the outcome of treatment; no pregnancy; no previous periodontal treatment and systemic antibiotics therapy in the last 6 months; not being smoker; the presence of at least two teeth with probing depths greater than 4 mm in two quadrants.
Exclusion criteria: the patient’s unwillingness to continue the treatment; failure to properly follow the researchers’ instructions; being under other treatment and taking medications which may affect the result.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Plaque index. Timepoint: Before the intervention, after six weeks and twelve weeks after the end of intervention,. Method of measurement: Observation of index score.;Pocket depth. Timepoint: Before the intervention, after six weeks and twelve weeks after the end of intervention,. Method of measurement: Probing in millimeter.;Attachment loss. Timepoint: Before the intervention, after six weeks and twelve weeks after the end of intervention,. Method of measurement: Probing in millimeter.;Bleeding of Probing (BOP). Timepoint: Before the intervention, after six weeks and twelve weeks after the end of intervention,. Method of measurement: Probing- No-unit.;Visual analogue scale. Timepoint: Immediately after intervention. Method of measurement: Questionnaire.
- Secondary Outcome Measures
Name Time Method