Evaluation of Outcomes of Coronary Artery Bypass Grafting.

  • STATUS
    Recruiting
  • End date
    Dec 20, 2023
  • participants needed
    1000
  • sponsor
    St. Petersburg State Pavlov Medical University
Updated on 23 January 2021

Summary

Evaluation of outcomes of coronary artery bypass grafting.

Description

Evaluation of outcomes of coronary artery bypass grafting (CABG) on-, off- pump, pump assisted as well as bimammary coronary artery bypass grafting.

Objective

To assess myocardial ischemic-reperfusion damage during different kinds of CABG.

To assess complications after during different kinds of CABG.

Details
Condition Coronary artery bypass graft, Vascular Diseases, Heart disease, Ischemic Heart Disease, Cardiac Ischemia, Myocardial Ischemia, Cardiac Disease, cabg, coronary artery bypass, coronary bypass, coronary artery bypass surgery
Treatment On-Pump CABG., Off-Pump CABG., Pump-assisted CABG.
Clinical Study IdentifierNCT03786939
SponsorSt. Petersburg State Pavlov Medical University
Last Modified on23 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 30 yrs and 80 yrs?
Gender: Male or Female
Do you have any of these conditions: Myocardial Ischemia or coronary bypass or Coronary artery bypass graft or Ischemic Heart Disease or Vascular Diseases or coronary artery bypass or Car...?
Ischemic heart disease with indications for coronary artery bypass grafting

Exclusion Criteria

valve disease
Clear my responses

How to participate?

Step 1 Connect with a site
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar
Name

Primary Contact

site
Name

Phone Email

0/250
Please verify that you are not a bot.

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...

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

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note