Actively Recruiting

Phase Not Applicable
Age: 30Years +
All Genders
NCT06745141

Myocardial Infarction and Periodontitis: Periodontal Health Intervention.

Led by Shanghai 10th People's Hospital · Updated on 2024-12-20

100

Participants Needed

1

Research Sites

265 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to establish a shared database of acute myocardial infarction patients with periodontitis, to clarify the clinical benefits of periodontitis intervention on acute myocardial infarction patients through simulated RCT study, and to establish a high-level database of acute myocardial infarction patients with periodontitis, so as to promote the application of oral health intervention in clinical practice.

CONDITIONS

Official Title

Myocardial Infarction and Periodontitis: Periodontal Health Intervention.

Who Can Participate

Age: 30Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients diagnosed with ST-segment elevation myocardial infarction (STEMI)
  • Severe periodontal disease with at least 5 teeth showing clinical attachment loss of 4 mm or more
  • Subgingival probing depth of 6 mm or more
  • At least 8 teeth with gingival bleeding on probing
  • Age 30 years or older
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Under 30 years old
  • HIV positive, chronic inflammation, tumor disease, drug dependence
  • Use of anticonvulsants or immunosuppressive agents
  • Pregnancy or lactation
  • Significant tooth loss with fewer than 8 remaining teeth
  • Long hospital stay over 10 days
  • New myocardial infarction before randomization
  • Presence of stent thrombosis
  • Refusal to sign informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shanghai Tenth People's Hospital

Shanghai, Shanghai Municipality, China, 200092

Actively Recruiting

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Research Team

J

Jiawen Wu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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