Effect of CI on Prognosis in the Elderly Patients With ACS

  • STATUS
    Recruiting
  • participants needed
    500
  • sponsor
    Beijing Friendship Hospital
Updated on 19 February 2024
cognitive impairment
mini-mental state examination
myocardial infarction
infarct
acute coronary syndrome
unstable angina
angina pectoris

Summary

This study aims to investigate the incidence and characteristics of cognitive Impairment(CI) in the elderly patients with acute coronary syndrome (ACS), and to determine whether CI are predictive of the prognosis of major adverse cardiovascular events (MACE) and mortality.

Details
Condition Acute Coronary Syndrome, Aged, Ischemic Heart Disease, Cognitive Impairment
Age 65years - 100years
Treatment MMSE and MoCA
Clinical Study IdentifierNCT04278911
SponsorBeijing Friendship Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

yr
Confirmed ACS diagnosis include unstable angina, ST-segment elevation myocardial infarction and Non ST-segment elevation myocardial infarction
fulfilled MMSE or MoCA
patients agreed and provided informed consent

Exclusion Criteria

Type 2 myocardial infarction and Acute nonischemic myocardial injury
past history of malignant tumors
Past history of stroke or dementia
Hepatic insufficiency (ALT8ULN or ALT3ULN and TBIL2ULN)
Renal insufficiency (GFR<15 ml/min/1.73m2)
Clear my responses

How to participate?

Step 1 Connect with a study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.