Health Condition 1: R888- Abnormal findings in other body fluids and substances
Conditions
Interventions
Intervention1: control group with healthy subjects: Subjects without any evidence of periodontal and systemic disease. Healthy control group where no sites with 3 mm probing pocket depth (PPD) and att
Sponsors
Neha Sahu
Eligibility
Inclusion criteria
Inclusion criteria: 1.Outpatients at the hospital within the age group of 18-60 years. 2.Person who are systemically healthy. 3.No history of anti-microbial therapy for the past three months. 4.Able to provide written informed consent and understand the study protocol
Exclusion criteria
Exclusion criteria: 1.Pregnant ladies and Lactating Mothers. 2.Patient with Smokeless tobacco habit. 3.Patients with history of systemic disease. Any underlying systemic disease will have effect on periodontal status. 4.Patients who have undergone periodontal therapy or antibiotic therapy in the past 6 months or any other drugs as there will be effect on the periodontal status. 5.Presence of any pre-existing oral infected condition. For e.g. pulpal pathosis. 6.Any patient undergoing radiation therapy. 7.History of any form of periodontal treatment in the past 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| There will be decrease in salivary IL-17 levels & ICTP levels in periodontitis patients & periodontitis patient having smoking habit after nonsurgical periodontal treatment.Timepoint: 1 year 6 month | — |
Secondary
| Measure | Time frame |
|---|---|
| Non-surgical periodontal treatment will have significant impact on bone resorption marker i.e IL-17 level & ICTP levels and will be well correlated with clinical parameters of periodontal tissue destruction.Timepoint: 1 year 6 month | — |
Countries
India
Contacts
Public ContactNeha Sahu
Department of periodontology and implantology, Government Dental College and Hospital, Raipur
Outcome results
None listed