Health Condition 1: K053- Chronic periodontitis Health Condition 2: Y998- Other external cause status
Conditions
Interventions
Sponsors
none
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who are willing to participate and sign the informed consent for this clinical trial. 2. Patients in the age group of 20 to 60 years. 3. Patients will be divided as: a) Group I-30 periodontally healthy patients,(PI and GI score between 0â??1.) and with no history/habit of smoking. b) Group II-30 periodontally healthy patients,(PI and GI score between 0â??1.) and with history/habit of smoking. c) Group III-30 patients with stage III or stage IV periodontitis, (affecting more than 30% of the teeth, with CAL >=5 mm, and PPD >=6mm) and with no history/habit of smoking. d) Group IV-30 patients with stage III or stage IV periodontitis ,(affecting more than 30% of the teeth, with CAL >=5 mm, and PPD >=6mm) and with history/habit of smoking.
Exclusion criteria
Exclusion criteria: 1.Systemic conditions associated with periodontal diseases. 2. History of periodontal treatment within the past 6 months. 3. Self-reported psychiatric disorder or psychotic medications. 4. Pregnancy or a history of taking medications known to increase the risk of gingival hyperplasia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate influence of anxiety and smoking in periodontally healthy, and periodontitis patients.Timepoint: baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) To evaluate the anxiety levels in periodontally healthy and periodontitis patients. 2) To evaluate the influence of smoking in periodontal disease severity. 3) To correlate the influence of anxiety and smoking in periodontally healthy and periodontitis patients Timepoint: baseline | — |
Countries
India
Contacts
Public ContactDr Abhay Kolte
VSPM Dental College and Research Centre
Outcome results
None listed