Health Condition 1: null- patients with chronic periodontitis Health Condition 2: R651- Systemic inflammatory response syndrome (SIRS) of non-infectious origin
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients willing to take part in the study. Subjects in the age group > 35 years without ant systemic disease Patients who have test teeth with both mesial and distal neighbouring teeth. Patients with more than 16 natural teeth. Patients with chronic periodontitis having a probing pocket depth of greater than 5 mm & radiographic evidence of bone loss Patients with no history of allergies.
Exclusion criteria
Exclusion criteria: Pregnant womans and lactating mothers. Teeth with both endo-perio lesions. Patients with use of tobacco or tobacco related products. Patients on antibiotics within 3 months prior to study. Patients having systemic diseases like diabetes mellitus, hypertension, bleeding disorders, hyperparathyroidism and compromised medical conditions. Patients who have had periodontal treatment in last six months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the present study was to evaluate the efficacy of Ornidazole, Curcumin gels and non-surgical periodontal therapy in chronic periodontitis patients, to evaluate their efficacy in suppressing the periodontopathogenic red complex micro organisms and also to evaluate their effect on periodontal clinical parameters.Timepoint: 0-3months at start of study | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome of the present study was to evaluate the efficacy of Ornidazole, Curcumin gels and non-surgical periodontal therapy in chronic periodontitis patients, to evaluate their efficacy in suppressing the periodontopathogenic red complex micro organisms and also to evaluate their effect on periodontal clinical parameters.Timepoint: 3months | — |
Countries
India
Contacts
St Joseph Dental College