Microcirculation

8

Review clinical trials related to Microcirculation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

CHECK-NIRS2D-Study

The study investigates how external, physiological, and behavioral factors influence the measurement of regional tissue oxygenation using two-dimensional near-infrared spectroscopy (NIRS) imaging in healthy volunteers. It aims to improve the standardization and reliability of this non-invasive method for assessing microvascular perfusion and tissue oxygenation. The study also examines the effects of temporary vascular occlusion, ambient temperature, physical activity, caffeine consumption, and nicotine consumption on NIRS-based tissue oxygenation measurements. The findings are intended to establish a standardized measurement protocol for future clinical research and the assessment of microvascular perfusion in critically ill patients.

Participants needed: 20
Trial details
Age: 20-40Biological sex: AllType: ObservationalSponsor: Heinrich-Heine University, DuesseldorfUpdated: Oct 2, 2026Locations: 1
Eligibility criteria

Healthy volunteers aged 20-40 years [+2]

Age below 20 years or above 40 years [+4]

Status: Not yet recruiting

Clinical Value of CT Perfusion in Peripheral Artery Disease

Peripheral artery disease (PAD) affects millions worldwide and can lead to serious complications such as leg ulcers, gangrene, and amputation. Current imaging methods mainly evaluate large blood vessels but do not measure microcirculation in the foot. Computed tomography perfusion (CTP) is a new technique that can assess blood flow in small vessels. The purpose of this study is to see whether combining CTP measurements with standard CT angiography images and patient clinical information can help predict which PAD patients are more likely to have poor outcomes after surgery to restore blood flow (revascularization). Poor outcomes include death or major limb problems such as amputation or need for another procedure. This is an observational study. Researchers will collect data from about 200 adult PAD patients who are scheduled to undergo revascularization. Participants will receive routine care including CT scans before and after surgery. No experimental drugs or devices are given. Researchers will follow participants for up to 2 years after surgery through medical records and phone calls to track their recovery and any complications. The results may help doctors identify high-risk patients earlier and improve treatment decisions.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Fudan UniversityUpdated: Sep 14, 2026
Eligibility criteria

Diagnosis of peripheral artery disease (PAD) confirmed by clinical evaluation an... [+3]

Allergy to iodinated contrast agents. [+5]

Status: Recruiting

ICU Combined Assessment of Cardio-Respiratory Exercise

This study aims to investigate how sepsis and critical illness can impair the cardiovascular system and microcirculation in intensive care unit (ICU) patients, which can lead to long-lasting muscle weakness/dysfunction or ICU-Acquired Weakness (ICU-AW) and exercise limitations.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of ManitobaUpdated: Jun 15, 2026Locations: 2
Eligibility criteria

Patients who have received mechanical ventilation for at least 7 days in the int...

Unable to provide consent [+8]

Status: Recruiting

Evaluation of the Microcirculatory Response to Fluids in Critically Ill Patients With Venous Congestion: A Prospective Observational Study

The hypothesis is that fluid-responsive patients who show signs of venous congestion experience a worsening of microcirculatory status after fluid administration compared to patients without signs of venous congestion

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Università Politecnica delle MarcheUpdated: Apr 2, 2026Locations: 1
Eligibility criteria

Critically ill patients admitted to the intensive care unit [+1]

Suspected or confirmed pregnancy [+1]

Status: Recruiting

Hemodynamic Evaluation Using Microcirculation for Early Treatment of Septic Patients

Despite early treatment, the deterioration and mortality of sepsis patients remains high. A possible explanation could be persistent tissue hypoperfusion, or undetected in the early phase despite the normalization of macro-hemodynamic parameters. This interventional study evaluates the impact of measuring microcirculation parameters by nurses on patient prognosis through early initiation of vascular filling.

Participants needed: 556
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, LimogesUpdated: Nov 21, 2025Locations: 6
Eligibility criteria

Age ≥ 18 years [+3]

Patient with arterial hypotension (SBP ≤ 100 mmHg) on admission [+4]

Status: Recruiting

The Impact of Intra-operative Fluid Infusion Rate on Microcirculation

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.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital Hradec KraloveUpdated: Mar 27, 2025Locations: 1
Eligibility criteria

elective recumbent and laparoscopic surgery [+1]

blood loss over 250 ml [+1]

Status: Recruiting

Urethral PeRfusion Index-Guided Hemodynamic ManagemenT in Patients Having Major Abdominal Surgery: the UPRIGHT Randomized Feasibility Trial

We will perform this single-center pilot trial to determine if the intraoperative urethral perfusion index is higher in patients assigned to maintaining postinduction baseline urethral perfusion index than in patients assigned to routine care (with blinded urethral perfusion index monitoring). As pre-planned substudies, we will also assess the agreement between a) urethral perfusion index-derived pulse rate and heart rate measured with an electrocardiogram and b) between the urethral perfusion index and the peripheral perfusion index.

Participants needed: 116
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: Universitätsklinikum Hamburg-EppendorfUpdated: Feb 21, 2025Locations: 2
Eligibility criteria

at least 45 years old [+3]

Pregnancy [+3]

Status: Not yet recruiting

Investigation of Novel and Established Therapies in a Human Intravenous Lipopolysaccharide Model of Sepsis

Sepsis is a common and life-threatening condition caused by a dysregulated host immune response to infection. Given the prominent role of endothelial breakdown and dysfunction in sepsis, therefore, there is an urgent need to establish strategies to protect the endothelium and preserve microcirculatory function. This study is a randomised clinical study investigating intravenous fluid therapy and oral imatinib therapy in healthy human volunteers exposed to intravenous lipopolysaccharide (LPS). The objective of the study is to investigate the biological effects of fluid and imatinib therapy on LPS-induced microcirculatory dysfunction.

Participants needed: 65
Trial details
Phase: Phase 1, Phase 2Age: 18-40Biological sex: AllType: InterventionalSponsor: Belfast Health and Social Care TrustUpdated: Oct 4, 2024
Eligibility criteria

Healthy adult volunteers aged between 18 and 40 years of age [+1]

Current participation in a clinical trial [+9]