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Hypotension clinical trials

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NCT ID: NCT05133817 Completed - Adverse Event Clinical Trials

Prophylactic Norepinephrine Infusion Combined With Colloid Coloading for Postspinal Anesthesia Hypotension

Start date: November 26, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the suitable infusion dose of prophylactic norepinephrine infusion combined with 6% Hydroxyethyl starch (130/0.4) coload for post-spinal anesthesia hypotension in patients undergoing cesarean section.

NCT ID: NCT05133271 Recruiting - Spinal Anesthesia Clinical Trials

Prediction of Maternal Arterial Hypotension After Spinal Anesthesia by Passive Leg Raise Test.

EDLIDL
Start date: February 3, 2021
Phase: N/A
Study type: Interventional

Spinal anesthesia for cesarean section is associated with a high incidence of low blood pressure. However, the pathophysiology of this arterial hypotension is not unequivocal and could involve, in addition to drug vasoplegia, a mechanical cause linked to lower caval compression or even true or relative hypovolemia. Passive leg raise test has been proposed in an attempt to identify parturients who are more likely to develop low blood pressure after spinal anesthesia. Nevertheless, the data available on this volume expansion test to predict hemodynamic variations after performing spinal anesthesia are still limited and few objective criteria have been described to predict this arterial hypotension. The objective of the research is to study the hypothesis according to which the presence of hypovolaemia (true or relative) objectified by a positive passive leg raise test would cause hypotension more frequent and more marked in intensity.

NCT ID: NCT05127876 Completed - Clinical trials for Spinal Induced Hypotension

Ephedrine Versus Ondansetron During Cesarean Delivery

Start date: January 10, 2022
Phase: Phase 4
Study type: Interventional

More than 30% of the patients receiving spinal anesthesia develop hypotension. Hypotension developed during cesarean section (C/S) under spinal anesthesia may jeopardize uteroplacental circulation leading to fetal compromise and even fetal death. The effect of prophylactic ondansetron on blood pressure after spinal anesthesia has not been compared in a clinical trial with that of a vasoconstrictor. The investigators will compare ephedrine and ondansetron for the prevention of maternal hypotension after spinal anesthesia for elective cesarean delivery.

NCT ID: NCT05120258 Not yet recruiting - Clinical trials for Post Spinal Hypotension

Can Subclavian / Infraclavicular Axillary Vein Collapsibility Index Predict Post-Spinal Hypotension in Caesarean Section Operations?

Cesarean
Start date: November 8, 2021
Phase:
Study type: Observational

Postspinal hypotension (PSH) is a common side effect with an incidence of 15.3% to 33%, which may result in organ hypoperfusion and ischemic events (1,2). In pregnant patients, this incidence may increase to 70% and severe PSH may increase the risk of maternal and fetal complications (3). Therefore, it is important for anesthesiologists to estimate the incidence of PSH in cesarean sections and to identify possible mechanisms (4). One of the important factors affecting the susceptibility of patients to intraoperative hypotension is the preoperative intravascular volume status. Recently, ultrasonography of the central veins has been used frequently by anesthesiologists in the preoperative period in order to evaluate the intravascular volume status (5). Salama and Elkashlan stated that the collapsibility index of the inferior vena cava is a new predictive value for PSH (6). Choi et al. showed that the subclavian vein or infraclavicular axillary vein collapsibility index is an important predictive value for hypotension after induction of general anesthesia (7). In this study, we wanted to investigate whether the subclavian vein or infraclavicular axillary vein collapsibility index can be used as a predictive value for PSH in cesarean section.

NCT ID: NCT05117151 Active, not recruiting - Clinical trials for Perioperative/Postoperative Complications

Ability of Hypotension Prediction Index to Predict Hypotension Events in Thoracic Surgery

Start date: March 23, 2022
Phase:
Study type: Observational

Investigators design this prospective observational study to exam the ability of hypotension prediction index in predicting intraoperative hypotension events in each phase of thoracic surgery

NCT ID: NCT05105477 Terminated - Clinical trials for Moderate to High-risk Noncardiac Surgery

Hypotension Prediction Index (HPI) SMART-BP Trial

Start date: November 17, 2021
Phase: N/A
Study type: Interventional

A multicenter, randomized comparison of intraoperative hemodynamic management with or without a protocolized strategy utilizing Hypotension Prediction Index (HPI) software guidance during moderate-to-high-risk noncardiac surgery.

NCT ID: NCT05101590 Completed - Clinical trials for Intraoperative Hypotension

Hypotension Decision Assist - Use, Safety and Efficacy

HDA-USE
Start date: October 22, 2021
Phase: N/A
Study type: Interventional

This clinical investigation will investigate whether Hypotension Decision Assist (HDA) is a feasible, safe and effective patient clinical decision support system to enhance an anaesthetist's ability to manage a patient's cardiovascular system when undergoing surgery. If successful, this study will provide evidence that the use of HDA facilitates beneficial outcomes for patients who have this device used.

NCT ID: NCT05101291 Completed - Anesthesia Clinical Trials

Fractional Spinal Anesthesia and Systemic Hemodynamics in Frail Elderly Hip Fracture Patients.

Start date: January 15, 2021
Phase: N/A
Study type: Interventional

Aging and frailty make the elderly patients susceptible to hypotension following spinal anaesthesia. The systemic haemodynamic effects of spinal anaesthesia are not well known. In this study, we examine the systemic haemodynamic effects of fractional spinal anaesthesia following intermittent microdosing of a local anesthetic and an opioid. We included 15 patients aged over 65 with considerable comorbidities, planned for emergency hip fracture repair. Patients received a spinal catheter and cardiac output monitoring using the LiDCOplus system. Invasive mean arterial pressure (MAP), cardiac index, systemic vascular resistance index, heart rate and stroke volume index were registered. Two doses of bupivacaine 2,25 mg and fentanyl 15µg were administered with 25 minutes in between. Hypotension was defined as a fall in MAP by >30% or a MAP <65 mmHg

NCT ID: NCT05101031 Completed - Clinical trials for Undifferentated Shock

Evaluation of Fluid Volume in Patients With Refractory Hypotension (Fresh-ER)

Fresh-ER
Start date: December 18, 2020
Phase:
Study type: Observational

The objective of the study is to observe the change in hemodynamic variables (i.e. CO, SV, HR, SV) as assessed during rapid fluid bolus.

NCT ID: NCT05092165 Recruiting - Acute Kidney Injury Clinical Trials

Methylene Blue for the Prevention of Hypotension During Hemodialysis

BLUE
Start date: October 21, 2021
Phase: Phase 2
Study type: Interventional

Hypotension is a common complication of intermittent renal replacement therapy. Methylene blue, an inhibitor of nitric oxide synthesis, has been suggested to improve hemodynamics during renal replacement therapy in ambulatory patients, but evidence is lacking for critically ill patients. This trial will assess whether methylene blue can improve hemodynamics and blood pressure for patients with shock requiring renal replacement therapy.