The evaluation of the effect of cocoa on periodontal disaese
Not Applicable
- Conditions
- Moderate Chronic Periodontitis.Chronic Periodontitis
- Registration Number
- IRCT201309303813N3
- Lead Sponsor
- Babol University of Medical Sience, Vice Chancellor for Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
The patients without history of systemic disease ; The patients without sensitivity to coca and it's products;The patients age between 30 to 50 ; The patients have chronic moderate periodontitis ;The patients be able to cooperate and have same plaque index; The patients without digestive problem
Exclusion criteria: smoker patients; menopause women;the patients who intake nutritional and vitamin supplements; the patients who cocoa and it's products are in they daily nutritional regiment; the patients whit any periodontal treatment during past 6 month; the patients whit antibiotic therapy during 1 month; the patients had taken anti inflammatory drugs during past 1 month.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total Antioxidant Power. Timepoint: At base line and One month after intervention. Method of measurement: Ferric Reducing Antioxidant power test-FRAP.;Saliva lipid preoxidation. Timepoint: At base line and One month after intervention. Method of measurement: Thiobarbituric Acid Reactive Substances test-TBARS.
- Secondary Outcome Measures
Name Time Method Gingival Index. Timepoint: this index will be recorded at base line and 2 , 4 ,6 and 8 weeks later. Method of measurement: loe and silness method.;Modified papillary bleeding index. Timepoint: this index will be recorded at base line and 2 , 4 ,6 and 8 weeks later. Method of measurement: Bernet method.;Probind pocket depth. Timepoint: this index will be recorded at base line and 2 , 4 ,6 and 8 weeks later. Method of measurement: whit periodontal probe.;Attachment loss. Timepoint: this index will be recorded at base line and 2 , 4 ,6 and 8 weeks later. Method of measurement: whit periodontal probe.