Chronic periodontitis. Chronic periodontitis
Conditions
Interventions
Intervention 1: Control group:SRP with placebo. Intervention 2: Intervention group:SRP with Mucoadhesive Locally Delivery Tetracycline 5%. Intervention 3: Intervention group:SRP with Tetracyclin 5%.
Placebo
Treatment - Drugs
Intervention group:SRP with Mucoadhesive Locally Delivery Tetracycline 5%
Intervention group:SRP with Tetracyclin 5%
Sponsors
Ethics committee of Kermanshah University of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to 60 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: patient free from systemic illness; patients who had note history of allergy to tetracycline; patiens having at least three sites with minimum 5 mm periodontal pocket; patient who had not taken antibiotic therapy and prophylaxy and periodontal therapy in the past 6 month Exlusion criteria: dissatisfaction and inability to comply with the follow-up visit requirments; history of systemic illness; received antibiotic treatment 2 weeks prior to study; pregnant and nursing patients
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Probing pocket depth. Timepoint: Baseline, two weeks, one and three months after the intervention. Method of measurement: Williams Periodontal Probe.;Clinical attachment loss. Timepoint: Baseline, two weeks, one and three months after the intervention. Method of measurement: Williams Periodontal Probe.;Plaque index. Timepoint: Baseline, two weeks, one and three months after the intervention. Method of measurement: plaque index Silness & Loe.;Gingival Index. Timepoint: Baseline, two weeks, one and three months after the intervention. Method of measurement: Observed.;Bleeding Index. Timepoint: Baseline, two weeks, one and three months after the intervention. Method of measurement: Observed\Bleeding Index Muhlemann. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMarzie Jamali
Kermanshah Dentistry School
Outcome results
None listed