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Clinical Trials/NCT04580706
NCT04580706
Unknown
N/A

The Effect of Frailty and Other Geriatric Syndromes on the Prognosis of Elderly Patients With Acute Coronary Syndrome

Beijing Friendship Hospital1 site in 1 country1,000 target enrollmentJanuary 1, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
ACS
Sponsor
Beijing Friendship Hospital
Enrollment
1000
Locations
1
Primary Endpoint
Death
Last Updated
5 years ago

Overview

Brief Summary

This is a prospective observational clinical trail which will recruit 1000-1500 participants over 65 years with frailty and acute coronary syndrome (ACS) in Beijing Friendship hospital. The investigators will conduct frailty assessment (FRAIL scale, CFS, SPPB), comorbidities, functional status (Barthel index, ADL, IADL), nutritional risk (MNA-SF), and then observe the clinical outcomes of elderly ACS participants with frailty. Then, the investigators will follow-up these participants separately in 1,3,6 and 12months, the anticipate follow-up time is 1 year. According to the follow-up results, investigators will evaluate the impact of frailty and other senile syndromes on the short-term and long-term prognosis of ACS, and develop a scoring system for the prognosis evaluation of elderly ACS participants.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
December 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sun Ying

Director of department geriatrics, Beijing Friendship Hospital

Beijing Friendship Hospital

Eligibility Criteria

Inclusion Criteria

  • Elderly participants over 65
  • Clinical diagnosis of acute coronary syndrome
  • Must be able to follow-up
  • Sign in the informed consent

Exclusion Criteria

  • Myocardial infarction caused by other acute disease
  • Mental disorders who cannot cooperate to complete the assessment
  • Severe liver dysfunction, kidney disease (CKD 5), end-stage malignant tumor
  • Totally disabled and bedridden

Outcomes

Primary Outcomes

Death

Time Frame: 1 year

All-cause death and cardiac death events

Major Adverse Cardiac and Cerebrovascular events

Time Frame: 1 year

Major Adverse Cardiac and Cerebrovascular events including heart failure, cardiac shock, malignant arrhythmia, myocardial infarction, revascularization, and cerebral infarction

Study Sites (1)

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