EFFECT OF SCALING ON SERUM hsCRP LEVELS AND PERIODONTAL PARAMETERS IN SYSTEMICALLY HEALTHY YOUNG WOMEN WITH GINGIVITIS
Gingivitis
About this trial
This is an interventional treatment trial for Gingivitis
Eligibility Criteria
Inclusion Criteria: females of reproductive age group (18-40 yrs) BMI (18.5 - 24.9) presence of ≥20 natural teeth Healthy periodontium (for control group) defined as bleeding on probing at < 10% of sites, with pockets ≤3 mm, no probing attachment loss and no radiologic bone loss. Gingivitis (17) (for test group) Gingivitis (intact periodontium) is defined as bleeding on probing at ≥ 10% of sites, with pockets ≤3 mm, no probing attachment loss and no radiologic bone loss. Gingivitis (reduced periodontium) is defined as bleeding on probing at ≥ 10% of sites with pockets ≤3 mm with possible probing attachment loss and possible radiologic bone loss. Localized gingivitis is defined as 10-30% of bleeding sites. Generalized gingivitis is defined as more than 30% of bleeding sites. Exclusion Criteria: history of androgen-secreting tumors, congenital adrenal hyperplasia and thyroid dysfunction nephrotic syndrome, chronic renal failure, significant cardiovascular disease, established type 1 or type 2 diabetes mellitus, active cancer within the last past 5 years smokers and alcoholics history of systemic antibiotics or oral contraceptives usage within last 3 months periapical pathology or oral inflammatory conditions other than gingivitis. any periodontal treatment within 6 months prior to study Patients with pockets ≥ 3 mm and probing attachment loss shall be excluded, hence, radiographic examination will not be needed.
Sites / Locations
- Post Graduate Institute of Dental Sciences
- Shikha Tewari
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
systemically healthy females with gingivitis
systemically and periodontally healthy females
scaling will be done at baseline
data will be recorded at baseline and no intervention will be done