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Effects of Non-surgical Periodontal Therapy on Cardiovascular Risk

Primary Purpose

Cardiovascular Diseases, Periodontitis

Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Non-surgical periodontal therapy
Control periodontal treatment
Sponsored by
Nanfang Hospital, Southern Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases focused on measuring Periodontitis, Non-surgical Periodontal Therapy, Cardiovascular risk

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 18 years;
  • At risk of cardiovascular disease (defined as "Framingham Score" predicted 10-year risk of cardiovascular disease ≥ 20%);
  • Moderate//severe periodontitis;

Exclusion Criteria:

  • Cardiovascular diseases at baseline (coronary heart disease, stroke and peripheral artery disease);
  • Received periodontal treatment within the past 6 months;
  • Pregnant or lactating females;
  • Non residents of Guangzhou and its surrounding cities or expected to leave Guangzhou or its surrounding cities within 1 year;
  • Malignant tumors or other end-stage diseases with life expectancy less than 1 year;
  • End-stage renal disease;
  • Patients with high bleeding risk, high blood pressures or other situations that make them unable to receive interventions;
  • Refuse to provide informed consent;

Sites / Locations

  • Stomatological Hospital, Southern Medical University
  • Nanfang Hospital, Southern Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Intervention arm

Control arm

Arm Description

Basic oral hygiene instructions. Full-mouth subgingival scaling and root planing under local anesthesia. Additional full-mouth subgingival scaling and root planing under local anesthesia every 3 months during the follow-up period if necessary.

Basic oral hygiene instructions. Full-mouth supragingival ultrasonic scaling.

Outcomes

Primary Outcome Measures

Change from Baseline Cardiovascular risk (Framingham risk score (FRS)) at 1 year.
Cardiovascular risk is assessed by "Framingham risk score (FRS)". (Circulation, 2008,117(6): 743-753.) Generally, the "Framingham risk score (FRS)" ranges from -4 to 33 for men and -5 to 33 for women. A higher "Framingham risk score (FRS)" means a higher risk of developing cardiovascular disease.

Secondary Outcome Measures

Change from baseline systolic blood pressure at 1 year after enrollment.
Change from baseline diastolic blood pressure at 1 year after enrollment.
Change from baseline fasting blood glucose at 1 year after enrollment.
Change from baseline glycosylated hemoglobin at 1 year after enrollment.
Change from baseline total cholesterol at 1 year after enrollment.
Change from baseline triglyceride at 1 year after enrollment.
Change from baseline low-density lipoprotein cholesterol at 1 year after enrollment.
Change from baseline high-density lipoprotein cholesterol at 1 year after enrollment.
Change from baseline high sensitivity C-reactive protein at 1 year after enrollment.
Change from baseline interleukin-6 at 1 year after enrollment.
Change from baseline cardiovascular risk (CHINA-PAR) at 1 year after enrollment.
China-PAR is an abbreviation of "Prediction for ASCVD Risk in China". It is a prediction model developed by YANG X. (Circulation, 2016,134(19):1430-1440.) Through China-PAR, the investigators can assess one's cardiovascular risk in 10 years. The result of China-PAR is directly one's predicted cardiovascular risk in 10 years, ranging from 0% - 100%, with a higher probability meaning a higher risk of cardiovascular disease.
Change from baseline community periodontal index at 1 year after enrollment.
Community periodontal index will be evaluated according to the guidelines by stomatologists. The community periodontal index ranges from 0 - 4 points for each tooth. Higher points mean more severe periodontitis.
Major adverse cardiovascular event
The major adverse cardiovascular event includes acute myocardial infarction, stroke, heart failure, peripheral artery disease, and coronary heart disease.
All-cause mortality
Defined as any death after enrollment.
Change from baseline anxiety at 1 year after enrollment.
Anxiety will be assessed through "Self-Rating Anxiety Scale (SAS)". The SAS score range from 20 - 80 points. Higher points mean more serious anxiety.
Change from baseline pain at 1 year after enrollment.
The degree of pain will be assessed through "Visual Analogue Scale (VAS)". The VAS score range from 0 - 10 points. Higher points mean more serious pain.

Full Information

First Posted
July 5, 2022
Last Updated
July 12, 2022
Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
Stomatological Hospital, Southern Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT05459727
Brief Title
Effects of Non-surgical Periodontal Therapy on Cardiovascular Risk
Official Title
Effects of Non-surgical Periodontal Therapy on Cardiovascular Risk in People at Risk of Cardiovascular Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
August 1, 2022 (Anticipated)
Primary Completion Date
August 31, 2025 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
Stomatological Hospital, Southern Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is to evaluate whether non-surgical periodontal therapy can help to control the cardiovascular risk among patients with moderate/severe periodontitis and at risk of cardiovascular disease.
Detailed Description
Previous studies showed that the treatment of periodontitis can partially improve the control of risk factors of cardiovascular disease (e.g. blood pressure, interleukin 6), whereas the evidence is still limited. Moreover, there is currently no study reporting the impact of periodontal treatment on the overall risk of cardiovascular disease. The prevalence of periodontitis in China was 62.4%. In clinical practice, a large number of patients with moderate/severe periodontitis and at risk of cardiovascular disease seek medical advice. However, the existing guidelines lack relevant recommendations. Therefore, this study intends to evaluate whether non-surgical periodontal therapy can help to control cardiovascular risk. 376 patients with moderate/severe periodontitis and at risk of cardiovascular disease will be randomized. Those randomized to the intervention arm will receive non-surgical periodontal therapy which includes full-mouth subgingival scaling and root planing. Those randomized to the control arm will receive supragingival ultrasonic scaling. All patients were given instructions on basic oral hygiene.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Periodontitis
Keywords
Periodontitis, Non-surgical Periodontal Therapy, Cardiovascular risk

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Masking Description
Due to the characteristics of the intervention in this trial, it would be impossible to blind the enrolled participants. However, the investigators and outcomes assessors will be blinded. Allocation to arms will be concealed in an envelope and revealed to the stomatologist and patient before delivering the first treatment. Other investigators like outcomes assessors and staff involved in the data collection and analyses will be masked.
Allocation
Randomized
Enrollment
376 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention arm
Arm Type
Experimental
Arm Description
Basic oral hygiene instructions. Full-mouth subgingival scaling and root planing under local anesthesia. Additional full-mouth subgingival scaling and root planing under local anesthesia every 3 months during the follow-up period if necessary.
Arm Title
Control arm
Arm Type
Placebo Comparator
Arm Description
Basic oral hygiene instructions. Full-mouth supragingival ultrasonic scaling.
Intervention Type
Procedure
Intervention Name(s)
Non-surgical periodontal therapy
Intervention Description
Non-surgical periodontal therapy includes basic oral hygiene instructions and full-mouth subgingival scaling and root planing under local anesthesia.
Intervention Type
Procedure
Intervention Name(s)
Control periodontal treatment
Intervention Description
Control periodontal treatment includes basic oral hygiene instructions and full-mouth supragingival ultrasonic scaling.
Primary Outcome Measure Information:
Title
Change from Baseline Cardiovascular risk (Framingham risk score (FRS)) at 1 year.
Description
Cardiovascular risk is assessed by "Framingham risk score (FRS)". (Circulation, 2008,117(6): 743-753.) Generally, the "Framingham risk score (FRS)" ranges from -4 to 33 for men and -5 to 33 for women. A higher "Framingham risk score (FRS)" means a higher risk of developing cardiovascular disease.
Time Frame
Baseline; 1 year
Secondary Outcome Measure Information:
Title
Change from baseline systolic blood pressure at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline diastolic blood pressure at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline fasting blood glucose at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline glycosylated hemoglobin at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline total cholesterol at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline triglyceride at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline low-density lipoprotein cholesterol at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline high-density lipoprotein cholesterol at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline high sensitivity C-reactive protein at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline interleukin-6 at 1 year after enrollment.
Time Frame
Baseline; 1 year
Title
Change from baseline cardiovascular risk (CHINA-PAR) at 1 year after enrollment.
Description
China-PAR is an abbreviation of "Prediction for ASCVD Risk in China". It is a prediction model developed by YANG X. (Circulation, 2016,134(19):1430-1440.) Through China-PAR, the investigators can assess one's cardiovascular risk in 10 years. The result of China-PAR is directly one's predicted cardiovascular risk in 10 years, ranging from 0% - 100%, with a higher probability meaning a higher risk of cardiovascular disease.
Time Frame
Baseline; 1 year
Title
Change from baseline community periodontal index at 1 year after enrollment.
Description
Community periodontal index will be evaluated according to the guidelines by stomatologists. The community periodontal index ranges from 0 - 4 points for each tooth. Higher points mean more severe periodontitis.
Time Frame
Baseline; 1 year
Title
Major adverse cardiovascular event
Description
The major adverse cardiovascular event includes acute myocardial infarction, stroke, heart failure, peripheral artery disease, and coronary heart disease.
Time Frame
Baseline; 3 months; 6 months; 9 months; 1 year; 2 years; 3 years;
Title
All-cause mortality
Description
Defined as any death after enrollment.
Time Frame
Baseline; 3 months; 6 months; 9 months; 1 year; 2 years; 3 years;
Title
Change from baseline anxiety at 1 year after enrollment.
Description
Anxiety will be assessed through "Self-Rating Anxiety Scale (SAS)". The SAS score range from 20 - 80 points. Higher points mean more serious anxiety.
Time Frame
Baseline; 1 year
Title
Change from baseline pain at 1 year after enrollment.
Description
The degree of pain will be assessed through "Visual Analogue Scale (VAS)". The VAS score range from 0 - 10 points. Higher points mean more serious pain.
Time Frame
Baseline; 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years; At risk of cardiovascular disease (defined as "Framingham Score" predicted 10-year risk of cardiovascular disease ≥ 20%); Moderate//severe periodontitis; Exclusion Criteria: Cardiovascular diseases at baseline (coronary heart disease, stroke and peripheral artery disease); Received periodontal treatment within the past 6 months; Pregnant or lactating females; Non residents of Guangzhou and its surrounding cities or expected to leave Guangzhou or its surrounding cities within 1 year; Malignant tumors or other end-stage diseases with life expectancy less than 1 year; End-stage renal disease; Patients with high bleeding risk, high blood pressures or other situations that make them unable to receive interventions; Refuse to provide informed consent;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiancheng Xiu, MD
Phone
+86-020-61648319
Email
xiujch@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiancheng Xiu, MD
Organizational Affiliation
Nanfang Hospital, Southern Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stomatological Hospital, Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510280
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jia Ni, MD
Email
441569008@qq.com
Facility Name
Nanfang Hospital, Southern Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510515
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Non-surgical Periodontal Therapy on Cardiovascular Risk

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