None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. For control group, the participants with at least 20 natural teeth and probing pocket depth of 2â??3 mm with no attachment loss and bleeding on probing with 2. For the study group, the participants had to have five qualifying sites in two quadrants with a minimum of two affected teeth in each quadrant with each site having probing depth >=5 mm, clinical attachment loss (CAL) >=3 mm, and bleeding on probing. 3. Patients who consented to willingly follow the endorsed plaque control and follow-up routine.
Exclusion criteria
Exclusion criteria: 1. Medically compromised patients with presence of any systematic disease 2. Pregnant & Lactating women 3. Patients taking any medication for the past 3 months. 4. Patients who are not maintaining their oral hygiene 5. Current smokers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of oral hygiene of the patient along with showing the importance of salivary biomarkersTimepoint: pre-op and one month following therapy | — |
Secondary
| Measure | Time frame |
|---|---|
| no evidence of disease progression and absence of disease after phase 1 non-surgical therapyTimepoint: one month after therapy | — |
Countries
India
Contacts
Banaras Hindu University