a Randomized Clinical Trial Evaluating the Effectiveness of Carbon Dioxide Use in Cardiac Surgery
- Conditions
- Carbon Dioxide
- Registration Number
- NCT04548687
- Lead Sponsor
- Meshalkin Research Institute of Pathology of Circulation
- Brief Summary
study of the efficacy and safety of carbon dioxide in cardiac surgery: repeated or minimally invasive
- Detailed Description
prospective randomized clinical single-center study of the efficacy and safety of using carbon dioxide in deaeration of cardiac cavities during cardiac surgery (repeated interventions and minimally invasive interventions)
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 120
- Planned cardiac surgery on the left heart with limited deaeration: Minimally invasive approach (mininotomy, minimally invasive lateral thoracotomy); Re-intervention
- Signed informed voluntary consent
- Patient refusal to participate in any stage of the study
- History of stroke, transient ischemic attack
- Hemodynamically significant stenosis of the brachiocephalic arteries (more than 70%)
- Swelling or thrombosis of the heart
- LV dysfunction (EF less than 30%)
- Atherosclerosis of the aorta (atheromatosis)
- Surgical access conversion
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method delirium: CAM-ICU, 3-D CAM 7 days after surgery positive test development of postoperative delirium: Richmond Agitation-Sedation Scale, Confusion Assessment Method-Intensive Care Unit (more than one error) - while in the intensive care unit; positive test the 3-Minute Diagnostic Interview for Confusion Assessment Method (CAM) defined delirium - while in the ward of the department: The CAM algorithm is considered positive if the following features are present: Feature 1) Acute onset or fluctuating course and Feature 2) Inattention and either Feature 3) Disorganized thinking or Feature 4) Altered level of consciousness.
- Secondary Outcome Measures
Name Time Method deaeration time intraoperatively deaeration time according to transesophageal echocardiography data
neurocognitive dysfunction 7 days after surgery development of neurocognitive dysfunction: Montreal Cognitive Assessment - two days before surgery and 7 days after surgery
Trial Locations
- Locations (1)
"E.Meshalkin National medical research center" of the Ministry of Health of the Russian Federation
🇷🇺Novosibirsk, Russian Federation
"E.Meshalkin National medical research center" of the Ministry of Health of the Russian Federation🇷🇺Novosibirsk, Russian FederationAlexander V. Bogachev-Prokophiev, MD, PhDContact+73833476029bogachev.prokophiev@gmail.comSergei A. BudagaevContact+73833476029ser.bud.med@gmail.com