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临床试验/NCT02150005
NCT02150005已完成不适用

Effects of Non-surgical Periodontal Treatment on Hemogram, Lipid and Glycemic Profiles of Patients With an Indication for Surgical Coronary Revascularization

Universidade Veiga de Almeida0 个研究点目标入组 22 人开始时间: 2009年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
22
主要终点
Hemocyte

研究概览

简要总结

Objective: The aim of this study was to examine the effects of non-surgical periodontal treatment on the hemogram, glycemic and lipid profiles in cardiopathic patients with an indication for surgical revascularization.

Materials and Methods: Twenty-two patients with chronic periodontitis, over 35 years of age (mean age 59.45 years) randomly assigned into 2 groups were evaluated. Test group (n=11), received periodontal treatment before the surgical procedure, and control group (n=11), did not received periodontal treatment prior to surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
35 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Undergoing cardiovascular treatment;
  • •Eight viable teeth in the oral cavity;
  • •Four periodontal sites with periodontal probing depths ≥5mm in different teeth.

排除标准

  • 未提供

研究组 & 干预措施

Periodontal treatment

Experimental

The test group received oral hygiene instructions, supragingival and subgingival scaling and root planning using curettes and an ultrasonic appliance.

干预措施: Periodontal treatment (Procedure)

Control

No Intervention

结局指标

主要结局

Hemocyte

时间窗: Baseline and 90 days after initial exam

Hemocyte presented a non-significant reduction in the test group. Mean difference 0.39 m/mcL

Reduction in probing depth in sites with PPD>3mm

时间窗: Baseline and 90 days after the initial exam

Reduction of 11.4% in probing depth in sites with Periodontal Probing Depth\>3mm

Reduction in probing depth in sites with PPD>5mm

时间窗: Baseline and 90 days after the initial exam

Reduction of 6.3% in probing depth in sites with Periodontal Probing Depth\>5mm

Reduction in probing depth in sites with CAL>3mm

时间窗: Baseline and 90 days after the initial exam

Reduction of 4.6% in probing depth in sites with Clinical Attachment Level \>3mm.

Reduction in probing depth in sites with CAL >5mm

时间窗: Baseline and 90 days after the initial exam

Reduction of 3.6% in probing depth in sites with Clinical Attachment Level \>5mm.

Leukocyte count

时间窗: Baseline and 90 days after the initial exam

Non-significant reduction of leukocyte count in the test group. Mean difference of 74.6 m/mcL.

Glucose

时间窗: Baseline and 90 days after the initial exam

Glucose showed a non-significant increase in the test group. Mean difference of 24.2 mg/dL.

Hemoglobin

时间窗: Baseline and 90 days after initial exam

Non-significant reduction in test group. Mean difference of 0.2 g/dL

Total Cholesterol

时间窗: Baseline and 90 days after initial exam

Significant reduction in the test group. Mean reduction of 27.4 mg/dL.

High density lipid

时间窗: Baseline and 90 days after initial exam

Significant reduction in test group. Mean difference of 8.2 mg/dL.

Low density lipid

时间窗: Baseline and 90 days after initial exam

Non-significant reduction in test group. Mean difference of 8.9 mg/dL.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Walmir Júnio de Pinho Reis Rodrigues

Researcher

Rio de Janeiro State University

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