Clinical Trials Directory

Trials / Unknown

UnknownNCT04244435

Neuroaxial Prophylaxis for CABG

Consequences of Using Thoracic Epidural Analgesia for Coronary Artery Bypass Grafting

Status
Unknown
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Volgograd State Medical University · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Investigators plan to study the effect of thoracic epidural analgesia on postoperative parameters (complication rate, duration of hospitalization, mortality, etc.) of coronary artery bypass grafting.

Detailed description

Investigators plan to conduct a comparative analysis of early postoperative complications of coronary artery bypass grafting with and without cardiopulmonary bypass in patients with independent risk factors for the development of postoperative complications (advanced age, diabetes mellitus, chronic kidney disease, obesity, chronic obstructive pulmonary disease) with various types of anesthesiology benefits (general anesthesia and thoracic epidural analgesia versus general anesthesia and opioids). Investigators predict a decrease in the risk of developing cardiac, respiratory, infectious and renal complications, a reduction in the duration of intensive care, inpatient treatment and mortality.

Conditions

Interventions

TypeNameDescription
PROCEDURECABGcoronary artery bypass grafting with and without cardiopulmonary bypass
DRUGthoracic epidural analgesiathoracic epidural analgesia at the level of 1-10 thoracic vertebrae (ropivacainum 0,2-0,5% 5-10 ml/h)
DRUGanalgesia of opioidsOpioids will be used for perioperative analgesia

Timeline

Start date
2020-02-01
Primary completion
2020-12-31
Completion
2022-01-31
First posted
2020-01-28
Last updated
2021-09-21

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT04244435. Inclusion in this directory is not an endorsement.