Health Condition 1: N186- End stage renal disease Health Condition 2: null- Group I - Chronic Periodontitis under hemodialysis for less than a year Group II - Chronic Periodontitis under hemodialysis for more than a year Group III - Chronic Periodontitis
Conditions
Interventions
Intervention1: Patients with Chronic Periodontitis and under hemodialysis for Less than a year: Scaling will be done using ultrasonic instruments and root planing will be done with Gracey Curettes Ed
Sponsors
Sheethel Menon V
Eligibility
Inclusion criteria
Inclusion criteria: A. Group I: Renal patients undergoing haemodialysis for less than a year with chronic periodontitis i. Patients with Chronic periodontitis will be diagnosed when there is attachment loss �5mm in more than 30% of teeth (according to the criteria of 1999 American Academy of Periodontology Workshop). ii. Patients with more than or equal to 20 teeth iii. Patients with clinical bleeding on probing. iv. Patients undergoing haemodialysis for atleast 3months and less than a year. B. Group II: 20 renal patients undergoing haemodialysis for more than a year with chronic periodontitis i. Patients with Chronic periodontitis will be diagnosed when there is attachment loss �5mm in more than 30% of teeth (according to the criteria of 1999 American Academy of Periodontology Workshop). ii. Patients with more than or equal to 20 teeth iii. Patients with clinical bleeding on probing. iv. Patients undergoing haemodialysis for more than a year. C. Group III: 20 systemically healthy periodontitis patients i. Patients with Chronic periodontitis will be diagnosed when there is attachment loss �5mm in more than 30% of teeth (according to the criteria of 1999 American Academy of Periodontology Workshop). ii. Patients with more than or equal to 20 teeth iii.Patients with clinical bleeding on probing.
Exclusion criteria
Exclusion criteria: 1.Individuals with uncontrolled hypertension inspite of medication 2.Edentulous patients 3.Smokers, alcoholics, pregnant women and lactating mothers. 4.Patients needing prophylactic antibiotic medication in association with periodontal probing. 5.Patients who had undergone periodontal treatment in the past 6 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1) C reactive protein level 2) Iron Indices - Serum Iron, Serum Ferritin, Total Iron binding capacityTimepoint: 1 month | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Plaque index 2) Gingival Index 3) Probing pocket depth 4) Clinical Attachment levelTimepoint: 1 month | — |
Countries
India
Contacts
Public ContactArun Sadasivan
Sree Mookambika Institute of Dental Sciences
Outcome results
None listed