Clinical Trials Directory

Trials / Unknown

UnknownNCT04306913

Outcome of Esmolol Potassium Cardioplegia Compared to Potassium Cardioplegia in Patients With Solitary Valvular Disease; Randomized Controlled Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Kasr El Aini Hospital · Academic / Other
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Perioperative myocardial injury remains one of the most serious complications of cardiac surgery. Numerous factors have been implicated during the pathogenesis process, including the technique of cardiac surgery, induction of cardioplegia and period of cardiac arrest. Lactic acid is the normal endpoint of the anaerobic breakdown of glucose in the tissues. The lactate exits the cells and is transported to the liver, thus it's considered to be an indicator of ischemia as it is produced by most tissues in the human body, with the highest level of production found in muscle. In any cardiac valve replacement surgery, patient must undergo cardiac bypass and arrest in diastole by using hyperkalemic cardioplegia solution; meanwhile the metabolism of myocardial cells is purely anaerobic. Esmolol an ultra-short beta blocker is supposed to decrease the anaerobic insult to the myocardial cells.

Conditions

Interventions

TypeNameDescription
DRUGEsmololesmolol 250 mg in cardioplegia solution every 25 minutes
DRUGPotassium Cardioplegic Solution15 meq potassium added to cardioplegia solution

Timeline

Start date
2020-04-01
Primary completion
2020-09-01
Completion
2020-09-01
First posted
2020-03-13
Last updated
2020-03-13

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04306913. Inclusion in this directory is not an endorsement.