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Hemodynamic Instability clinical trials

View clinical trials related to Hemodynamic Instability.

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NCT ID: NCT04428372 Recruiting - Clinical trials for Hemodynamic Instability

MAnnitol for Blood Pressure Stability in HemoDialysis (MAP-HD)

Start date: April 6, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

This proposal will measure the effects of mannitol administration versus placebo in hypotensive-prone, adult, maintenance hemodialysis patients with respect to changes in patient symptoms and blood pressure stability.

NCT ID: NCT04319965 Recruiting - Critical Illness Clinical Trials

Complications Related to Transpulmonary Thermodilution

COTRADIL
Start date: February 8, 2020
Phase:
Study type: Observational

The transpulmonary thermodilution is commonly used in patients with acute circulatory failure in the intensive care unit and for monitoring surgical patients at high risk. However, the incidence of complications and their risk factors in patients monitored by transpulmonary thermodilution has not been completely reported yet.

NCT ID: NCT04264286 Recruiting - Clinical trials for Hemodynamic Instability

The Effects of Esmolol on the Hemodynamic Response to Orotracheal Extubation

Start date: July 1, 2019
Phase: Phase 4
Study type: Interventional

Beta-blockers are useful tools for the prevention of hemodynamic instability in the manipulation of airways. The main objective of the present study is to evaluate the effectiveness of using esmolol in attenuating hemodynamic responses at the time of tracheal extubation, by assessing the incidence of tachycardia in relation to placebo.

NCT ID: NCT04010058 Recruiting - Clinical trials for Hemodynamic Instability

Postoperative Continuous Non-invasive Haemodynamic Monitoring on the Ward

PostConMon
Start date: September 2, 2019
Phase: N/A
Study type: Interventional

The patient's clinical care will not be altered apart from an the use of a non-invasive monitor for a short time, without any biological sample acquisition, or follow-up. This is low risk. The device works through a complex pressure measurement in the fingers and by slightly squashing the fingers it can cause minor impairments to circulation. This represents a very small risk. To mitigate this risk the investigators will exclude patients with impaired circulation to the fingers and fingers will be monitored. The approach is necessarily on the day of surgery and for many people this is an anxious time. The investigators have a lot of experience of approaching patients on the day of surgery for providing consent for observational studies - the investigators use caution and sensitivity. The investigators do not approach patients who the clinical team consider anxious or where there is significant pressure on time.

NCT ID: NCT03864094 Recruiting - Clinical trials for Hemodynamic Instability

Hemodynamics During Induction of General Anesthesia After Prophylactic Ephedrine, Phenylephrine or Norepinephrine.

VH
Start date: March 15, 2022
Phase: Phase 4
Study type: Interventional

In this trial the investigators want to examine if there is any difference in hemodynamic stability when giving equipotent prophylactic injections of ephedrine 0,1 mg/kg, phenylephrine 1 microg/kg, norepinephrine 0,1 microg/kg or sodium chloride (NaCl) 9 mg/ml during induction of general anesthesia with propofol and remifentanil.

NCT ID: NCT03617978 Recruiting - Clinical trials for Hemodynamic Instability

Passive Leg Raise During Cardiopulmonary Resuscitation

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

during cardiopulmonary resuscitation, an important element of the procedure is to achieve optimal organ perfusion. For this purpose, high quality chest compressions is one of the basic elements of the procedure. however, similarly as in the case of hypovolemic shock, elevation of the lower limbs may be helpful. The study is a randomized cross-over study and includes the effect of lower limb elevation on hemodynamic parameters in healthy participants.

NCT ID: NCT03612492 Recruiting - Clinical trials for Hemodynamic Instability

The Effects of Lidocaine and Esmolol on Attenuation of Hemodynamic Response to Orotracheal Intubation

Start date: July 1, 2018
Phase: Phase 4
Study type: Interventional

The present study aims to compare the hemodynamic response during laryngoscopy and orotracheal intubation using continuous infusion of lidocaine and esmolol in patients undergoing general anesthesia.

NCT ID: NCT03592290 Recruiting - Clinical trials for Hemodynamic Instability

Hemodynamics Monitoring During Lower Body Negative Pressure (LBNP) Induced Controlled Hypovolemia

LBPN
Start date: November 15, 2017
Phase:
Study type: Observational

To monitor the changes in central and peripheral monitors/waveforms during gradual hypovolemia induced by lower body negative pressure in healthy volunteers.

NCT ID: NCT03113435 Recruiting - Clinical trials for Hemodynamic Instability

Patient Management During Major Abdominal Surgery: an Oxygen Consumption Protocol Compared to Standard Approach

HEART-CORE
Start date: June 1, 2018
Phase: N/A
Study type: Interventional

This study compares the actual standard of care with a new protocol to guide hemodynamic optimization during major abdominal surgery, which is more tailored on patient real needs. During general anesthesia metabolic needs of the body are markedly reduced and increase in CO may not be necessary. In addition, excessive fluid administration has been related to worse post-operative outcomes. We divide patients into three groups: the standard treatment group, the NICE protocol group and the intervention group. In this group we use the v-aCO2/CaO2-CvO2 as marker of tissue ability to increase their oxygen consumption in response to increased O2 delivery, and based on this index the administration of fluid. The principal aim is to optimize functional hemodynamics in order to reduce the fluid balance at the end of the surgery.

NCT ID: NCT02891577 Recruiting - Clinical trials for Hemodynamic Instability

Study of Ultrasonographic Cava Femoral Ratio in the Critically Ill Patient With Shock

ECHO-RCF
Start date: March 2016
Phase: N/A
Study type: Observational

This study aims to describe the ratio of the diameter of inferior vena cava to the common femoral vein measured by ultrasonography in critically ill patients with shock, and to evaluate the potential link between this ratio and the existence of intra-abdominal disease.