Clinical Trials Directory

Trials / Completed

CompletedNCT02417376

Changes in the Risk Factors of Coronary Heart Disease Observed After Scaling and Root Planing

Effect of Nonsurgical Periodontal Treatment on Systemic Risk Markers of Cardiovascular Disease Clinically and Biochemically: A Randomized Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Government College of Dentistry, Indore · Academic / Other
Sex
All
Age
35 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether scaling and root planing as a periodontal intervention helps in improving the overall health of patients suffering from coronary heart disease.

Detailed description

This study is a randomized, outcome assessor blinded, parallel group, trial to evaluate the effect of non surgical periodontal treatment in the form of scaling and root planing on coronary heart disease patients. 70 clinically defined coronary heart disease (CHD) patients with mild to moderate periodontitis, were allocated into two groups- experimental and control, in a ratio of 1:1. Scaling and root planing was provided as the intervention to the experimental group. To the control group no periodontal intervention in any form was provided. The primary outcome assessed is the changes in C-reactive protein level at baseline and after 1, 3, and 6 months of periodontal intervention. The secondary outcomes assessed are lipid profile, white blood cells (WBC) profile, and blood pressure (systolic and diastolic) at baseline and after 1, 3, and 6 months of periodontal intervention. Periodontal parameters including plaque index (PI), gingival index (GI), bleeding on probing (BOP), periodontal probing depth (PPD), and clinical attachment loss (CAL) is also assessed at baseline and after 6 months. All these parameters were also compared with their corresponding values in the control group.

Conditions

Interventions

TypeNameDescription
DEVICEpiezoelectric ultrasonic scaler (frequency of 28-36 KHz)Periodontal treatment in the form of scaling and root planing (SRP) is provided to the patients assigned to the experimental group, after baseline examination. Scaling is performed using piezoelectric ultrasonic scaler (frequency of 28-36 KHz) and root planing is performed using area specific Gracey curettes (set of 7 instruments number #1-14). SRP is completed in two appointments of 45 min to 1 hour, within 24 hours period.
DEVICEGracey curettesset of 7 instruments number #1-14

Timeline

Start date
2013-05-01
Primary completion
2014-10-01
Completion
2014-10-01
First posted
2015-04-15
Last updated
2017-02-24
Results posted
2017-02-24

Source: ClinicalTrials.gov record NCT02417376. Inclusion in this directory is not an endorsement.