Effect of Tetracycline in the treatment of chronic periodontitis
Phase 2
- Conditions
- Chronic periodontitis.Chronic periodontitis
- Registration Number
- IRCT2016030226872N1
- Lead Sponsor
- Ethics committee of Kermanshah University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 75
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
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method