Telemedicine Follow-up for Post-ACS Patients

  • STATUS
    Recruiting
  • participants needed
    88
  • sponsor
    Tomsk National Research Medical Center of the Russian Academy of Sciences
Send
Updated on 5 August 2020
See if I qualify
acute coronary syndrome

Summary

The aim is to compare the safety of using telemedicine and office visit follow-up in post-acute coronary syndrome patients

Description

Rehabilitation after acute coronary syndrome includes visits to the cardiologist's office at 1, 2, 6 and 12 months after discharge. Due to the Covid-19 pandemic, visiting a cardiologist's office maybe impossible. In such cases telemedicine follow-up visit would be reasonable choice. Taking into account the absence of studies in this area, providing investigation evaluating parameters of safety for both methodics is relevant.

Details
Condition Acute Coronary Syndrome
Age 40years - 100years
Treatment Telemedicine FU, Office FU
Clinical Study IdentifierNCT04485754
SponsorTomsk National Research Medical Center of the Russian Academy of Sciences
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Signed informed consent
Age 40 years
PCI with coronary artery stenting for ACS
Angiographic success PCI

Exclusion Criteria

Patients with cancer
Severe CHF (EF LV <35% or functional class of heart failure III-IV NYHA)
Severe valvular heart disease or Prosthetic heart valves
Severe forms of CKD (GFR<30mL/min)
Planned staged revascularization during the next 12 months
Planned surgery within the next 12 months
Clear my responses
Read more

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team

Email

View email

Phone

Phone country flag

View phone
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

Browse trials for

acute coronary syndrome

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.