Moderate chronic periodontitis. Chronic periodontitis
Conditions
Interventions
Intervention 1: Er:YAG laser (Fotona-fidelis plus Ljubljana-Slovenia) with following characteristic: Wave length: 2490nm
Energy level: 160 mJ/pulse
Fiber tip: chisel shape
Hand piece: Ro14. Intervention 2: Ultrasound scaler (UDS-K 2012, Guilin woodpeker Medical instrument co) with following characteristic: output half-excursion force: more than 2N
output tip vibration frequency: 28kHz±3kHz
water pressure: 0.1bar to 5bar.
Treatment - Other
Er:YAG laser (Fotona-fidelis plus Ljubljana-Slovenia) with following characteristic: Wave length: 2490nm
Hand piece: Ro14.
Ultrasound scaler (UDS-K 2012, Guilin woodpeker Medical instrument co) with following characteristic: output half-excursion force: more than 2N
Sponsors
Vice of Research, School of Dentistry, Isfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: 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.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Jaber Yaghini
Periodontal Department, School of Dentistry, Isfahan University of Medical Sciences
Outcome results
None listed