None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients free from systemic diseases between the age group of 18-70 years, who signed the consent form, having a habit of tobacco consumption and undergoing non-surgical periodontal therapy were a part of this clinical trial.
Exclusion criteria
Exclusion criteria: Patients giving a history of undergoing surgical periodontal treatment in the past 6 months, as well as pregnant or lactating women, were excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. To evaluate the efficacy of oral antioxidant supplement as an adjunt to scaling and root planing in the non-surgical management of Periodontal Disease in Tobacco Users 2. To evaluate the efficacy of scaling and root planing in the non-surgical management of Periodontal Disease in Tobacco Users 3. To compare the efficacy of oral antioxidant supplement as an adjunt to scaling and root planing versus scaling and root planing alone in the non-surgical management of Periodontal Disease in Tobacco Users Timepoint: Baseline and after 15 days | — |
Secondary
| Measure | Time frame |
|---|---|
| The clinical parameters evaluated were- Oral Hygiene Index- Simplified(OHI-S), Plaque Index(PI), Gingival Index(GI), Modified Sulcular Bleeding Index (M-SBI), Pocket probing depth (PPD) and Clinical Attachment Level (CAL).Timepoint: Baseline and after 15 days | — |
Countries
India
Contacts
Terna Dental College