Health Condition 1: Z006- Encounter for examination for normal comparison and control in clinical research program
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients willing to voluntarily participate with minimum of 20 functional natural teeth and patients with moderate to severe form of periodontitis with at least two teeth with periodontal pocket depth more than or equal to 6mm and clinical attachment level more than or equal to 3mm
Exclusion criteria
Exclusion criteria: 1. Subjects allergic to sulfonated compounds. 2. Subjects with any systemic disorders 3. Subjects who have used antibiotics or anti-inflammatory drugs for last 3months. 4. Pregnant and lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome in the present study will be the reduction in pocket probing depth and gain in clinical attachment levels in test groupsTimepoint: 15 days and 3rd month | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome will be the reduction in inflammatory mediators (Interleukin 1β and TNF- α) in test groupsTimepoint: 15 days and 3rd month | — |
Countries
India
Contacts
Manipal College of Dental Sciences