Clinical Trials Logo

Myocardial Protection clinical trials

View clinical trials related to Myocardial Protection.

Filter by:
  • None
  • Page 1

NCT ID: NCT06287372 Completed - Cardiac Surgery Clinical Trials

Comparison of Changes in Intra-myocardial Amino Acids During Use of Calafiore and Modified Del Nido Cardioplegia

Start date: July 4, 2022
Phase:
Study type: Observational [Patient Registry]

The aim of the present study was to investigate intra-operative changes in markers of myocardial injury and myocardial intracellular amino acids during ischemia and reperfusion, comparing two methods of myocardial protection; Calafiore intermittent antegrade warm blood cardioplegia or modified del Nido intermittent antegrade cold blood cardioplegia in routine coronary artery bypass grafting procedures.

NCT ID: NCT04231903 Completed - Clinical trials for Mitral Valve Prolapse

Myocardial Protection in Minimally Invasive Mitral Valve Surgery

Start date: June 1, 2014
Phase:
Study type: Observational

Perfusion strategies and aortic clamping techniques for right mini-thoracotomy mitral valve (MV) surgery have evolved over time and remarkable short- and long-term results have been re-ported. However, some concerns have emerged about the adequacy of myocardial protection dur-ing the minimally invasive approach and about the role of aortic clamping strategies in this contest. Aim of this study was to compare the efficacy, in terms of myocardial protection, of the en-do-aortic clamp (EAC) versus the trans-thoracic aortic clamp (TTC) in patients undergoing right mini-thoracotomy MV repair. A single center, prospective observational study was performed between June 2014 to June 2018 on patients undergoing right mini-thoracotomy MV repair with retrograde arterial perfusion and EAC or TTC. The selection of one setting in respect to the other was patient orientated. Myocardial protection was assessed through creatinine kinase-myocardial band (CK-MB) and cardiac Troponin T (cTn-T) blood levels immediately after the surgical procedure and at 6, 12, and 24 hours and compared between the two groups.

NCT ID: NCT03859115 Completed - Clinical trials for Myocardial Protection

Effects of TENS on Myocardial Protection in Patients Undergoing AVR

Start date: March 15, 2019
Phase: N/A
Study type: Interventional

Patients undergoing aortic valve replacement are randomized to receive TENS (transcutaneous electrical nerve stimulation) or sham stimulation at one arm for 30 min under various anesthetic conditions: no anesthesia (preanesthesia), sevoflurane or propofol anesthesia. Cardioprotective effects of TENS are compared through Langendorff rat heart perfusion system using plasma dialysate from patients.

NCT ID: NCT03595111 Not yet recruiting - Clinical trials for Myocardial Protection

Myocardial Biopsy in Congenital Cardiac Surgery

Start date: July 2018
Phase: N/A
Study type: Interventional

Despite major advances in the technical aspects of surgical repair of congenital heart diseases, perioperative myocardial damage with low cardiac output remains the most common cause of morbidity and death after repair of congenital heart lesions.

NCT ID: NCT01941459 Completed - Clinical trials for Myocardial Protection

Comparison of Blood Cardioplegia and Custodiol

Start date: March 2007
Phase: N/A
Study type: Observational

Thru the last 20 years it has been a discussion witch solution that gives the best myocardial protection during cardiac arrest by heart operations. - It has been a tendency that a blood based cardioplegia gives a better protection bye long ischemic times but it has not been possible too conclude in this matter. - The investigators have two groups of cardioplegia, the blood based and, the crystalloid based cardioplegia. - It has been done a lot of studies to see what kind of cardioplegia that gives the best myocardial protection. Different temperature, different amount and content, retrograde or antegrade or both, contentiously and further on have been tested without a clear conclusion. - The investigators decided to make a study with a cohort of patients as homogenous as possible with a cross clamp time around 70 min. - Adult patients' with a severe aortic stenoses without any other significant heart disease was included in our prospective randomised study. - Patients with additional significant coronary artery disease (≥ 50% stenoses) were excluded from the study. - The investigators used the well known biomarkers CK-MB and troponin-T too evaluate the myocardial damage.

NCT ID: NCT01941420 Completed - Aortic Stenosis Clinical Trials

Comparison of Blood and Crystalloid Cardioplegia

Start date: November 2006
Phase: N/A
Study type: Observational [Patient Registry]

The investigators decided to make a study with a cohort of patients as homogenous as possible with a cross clamp time around 70 min. Adult patients with a severe aortic stenoses without any other significant heart disease was included in our prospective randomised study. This group of patients was chosen for two reasons. First, these patients have left ventricular hypertrophy making the myocardium vulnerable to ischemia, secondly the investigators wanted to avoid the possible confounding effect of ischemia found in patients with variable degrees of coronary artery disease. Therefore, patients with additional significant coronary artery disease (≥ 50% stenoses) were excluded from the study.

NCT ID: NCT00610350 Completed - Clinical trials for Myocardial Protection

Levosimendan and Myocardial Protection

Start date: January 2005
Phase: Phase 4
Study type: Interventional

The aim of this study is to investigate whether pharmacological pre-treatment with levosimendan reduces intensive care unit (ICU) length of stay in patients undergoing elective myocardial revascularization under cardiopulmonary bypass.

NCT ID: NCT00546390 Completed - Clinical trials for Remote Ischemic Preconditioning

Protection of the Heart With Remote Ischemic Preconditioning During Heart Surgery: A Pilot Study

Start date: November 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a treatment called remote ischemic preconditioning (rIP) to no treatment. rIP is a simple treatment that is believed to help patients recover better after heart surgery. This treatment involves applying a large blood pressure cuff to one leg. The blood pressure cuffs will be inflated for 5 minutes and then deflated for 5 minutes. This will be done 4 times in a row.