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Microcirculation clinical trials

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NCT ID: NCT06368635 Recruiting - Clinical trials for Coronary Artery Disease

The Cerebral Microcirculation Diseases and Coronary Microcirculation Disease Study

CCMD
Start date: January 1, 2024
Phase:
Study type: Observational

Ischaemic heart disease (IHD) and degenerative brain disease are two major sources of death and disability affecting all countries. While the consequences of obstructive disease in major vessels supplying blood to both organs have been widely documented, less attention has been paid to disease processes affecting the microcirculation that may affect cardiac and cerebral function. Yet, over the last decade significant progress has been made in understanding the substrate of microvascular disease in both organs. In the heart, arteriolar thickening and capillary rarefaction that reduce the conductance of the microvasculature and its ability to vasodilate in response to increased myocardial oxygen demands constitute the leading cause of coronary microvascular dysfunction (CMD). In the brain, concentric hyaline thickening of deep penetrating small arteries (arteriolosclerosis) with associated fibrosis of the vessel wall constitutes the most frequent substrate for cerebral small vessel disease (CSVD). Of note, both CMD and CSVD share common risk factors, such as age, hypertension, and diabetes.3 These factors might have a common effect on the microvascular domain of cardiac and cerebral vascular beds. Although a potential link between both conditions has been hypothesized based on the similarities between pathological changes and risk factors, advance in knowledge exploring this has been hampered by lacking objective evidence of CMD and pathological brain changes indicative of CSVD in prior research studies. Thus, the relationship between CMD and CSVD is unknown. The main objective of this study was to analyse the relationship between cerebrovascular disease and CMD in patients with atherosclerotic coronary artery disease (CAD).

NCT ID: NCT06141681 Recruiting - Microcirculation Clinical Trials

Evaluation of Microcirculation With Photoplethysmography (Pulse Oximetry) in Healthy Volunteers and Ventilated Patients

Start date: June 19, 2023
Phase:
Study type: Observational

The objective of this observational study is to explore microcirculation in healthy volunteers and in ventilated patients in the operating room and in critical care. The general objective of this study is to evaluate microcirculation with photoplethysmography (PPG) in different pathophysiological situations and to compare PPG with available standard methods. Specifically, evaluate the correlation between the determinations of AC-DC waves obtained by Photoplethysmography (PPG) and those obtained in different dynamic tests in healthy volunteers. To compare microcirculation assessments [capillary refill time (CRT), perfusion index (PI), perfusion index variability (PIV)] with measurements obtained by PPG in the context of critically ill patients. To compare microcirculation assessments (CRT, PI PVI) with measurements obtained by PPG in the context of patients on invasive mechanical ventilation (IMV) in the operating room and in critical care.

NCT ID: NCT05681052 Recruiting - Septic Shock Clinical Trials

Mottling Score and Central Venous Oxygen Saturation in Septic Shock Patients

Start date: October 1, 2022
Phase:
Study type: Observational

Mottling score and central venous oxygen saturation are described as a clinical evaluation of tissue perfusion. This study describes mottling incidence and mottling score in septic shock patients according to central venous oxygen saturation.

NCT ID: NCT05606536 Recruiting - Microcirculation Clinical Trials

The Impact of Intra-operative Fluid Infusion Rate on Microcirculation

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

Intraoperative fluid therapy (IFT) is an integral part of anesthesia care during surgery. Its main indication is the optimization of oxygen supply to the tissues. For elective surgery that is not associated with higher blood loss and a long period of preoperative fasting, including fluids IFT is dosed to cover the basal daily need for fluids. However, it is not clear whether this fluid dose is optimal. Surgery is a stress factor that leads, among other things, to damage of the endothelial glycocalyx (EG). EG binds a significant amount of plasma, which is released during EG destruction and causes relative hemodilution. Isovolumic hemodilution is an established intraoperative procedure that serves to better control bleeding in procedures where bleeding is expected. However, partial hemodilution occurs even with standard IFT, and even when fluids are hardly given at all. Flow parameters in microcirculation have not yet been described depending on IFT conduction. The parameters of the microcirculation reflect its functioning, which will consequently affect the postoperative phase of the patient's moaning and clinical outcome.

NCT ID: NCT04397640 Recruiting - Sepsis Clinical Trials

Myocardial Contrast Echocardiography in Septic Patients

Start date: January 31, 2020
Phase: N/A
Study type: Interventional

Myocardial microcirculatory alterations may be involved in the pathogenesis of acute cardiac dysfunction or septic cardiomyopathy in septic patients. The investigators study the cardiac function (systolic and diastolic) with two-dimensional echocardiography (TTE), and the myocardial microcirculation with contrast echocardiography (MCE) and sulphur hexafluoride microbubbles Sonovue injection in ICU septic patients.

NCT ID: NCT04346290 Recruiting - Kidney Transplant Clinical Trials

Effects of Dexmedetomidine on Microcirculation and Residual Kidney Function in Kidney Donors

Start date: July 24, 2020
Phase: Phase 4
Study type: Interventional

Kidney transplant can help patients with end-stage kidney disease to get rid of dialysis and have a good quality life. However, during the renal donation operation, the stress response and subsequent inflammatory responses may result in damage to the residual kidney and transplanted kidney. Dexmedetomidine can increase urine output and decrease the neutrophil gelatinase associated lipocalin level in patients receiving coronary artery bypass surgery. The primary goal of this trial is to investigate the effects of perioperative infusion of dexmedetomidine on the microcirculation and residual kidney function in kidney donors and on the transplanted kidney function in kidney recipients.

NCT ID: NCT04294316 Recruiting - Microcirculation Clinical Trials

Enhanced-contrast Brain Ultrasound in Cardiorespiratory Arrest

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Brain microcirculation alterations may be involved in comatose patients and non-survivors after cardiorespiratory arrest. For a three day-period, we investigate brain microcirculation using contrast-enhanced ultrasound with contrast Sonovue injection in patients with successful resuscitation after out-hospital or in-hospital cardiorespiratory arrest.

NCT ID: NCT04290767 Recruiting - Shock Clinical Trials

Brain Ultrasound With Contrast Microbubbles Injection in Shock Status

Start date: March 6, 2019
Phase: N/A
Study type: Interventional

Alterations in the brain microcirculation may be involved in patients with shock. For a three-day period, we investigate the brain microcirculation using contrast-enhanced ultrasound with microbubble injection in patients with septic and non-septic shock.Ultrasound examination is performed daily to estimate global cerebral blood flow, and to evaluate the brain microcirculation, using variables of the time-intensity brain perfusion curve, after sulphur hexafluoride microbubble Sonovue injection.

NCT ID: NCT01204554 Recruiting - Microcirculation Clinical Trials

Microcirculation in Perforator Flaps. Enhancing Tissue Survival

Start date: September 2008
Phase: Phase 0
Study type: Interventional

The aim of the present study is to assess the microcirculatory changes in the distal part of the perforator flap using ICG fluorescence angiography.

NCT ID: NCT00484133 Recruiting - Severe Sepsis Clinical Trials

Microcirculation Guided Therapy Versus "Standard Treatment" of Severe Sepsis

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to asses the recovery of organ failure between two resuscitation protocols in severe sepsis: standard, pressure guided therapy versus a microcirculation guided therapy