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Hemodynamics Instability clinical trials

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NCT ID: NCT06385756 Not yet recruiting - Clinical trials for Hemodynamics Instability

Effect of Amobarbital Sodium Combined With Low-dose Propofol on Hemodynamics During Induction and Perioperative Adverse Reactions

Start date: May 1, 2024
Phase: Phase 4
Study type: Interventional

At present, there are limited data on perioperative efficacy of barbiturates at home and abroad. The purpose of this clinical trial is to observe the effects of amobarbital sodium combined with low-dose propofol on hemodynamics during induction and perioperative adverse reactions in gynecological laparoscopic surgery patients, and to provide a more reasonable, safe and comfortable anesthesia program for female patients who undergoing laparoscopic surgery. The main questions it aims to answer are: - whether the combination of the two results on more stable hemodynamics during induction in gynecological laparoscopic surgery patients; - whether the incidence of perioperative oxidative stress and inflammation and postoperative nausea and vomiting(ponv) improved after the use of the two combinations of anesthesia induction. Participants will: - Induction of anesthesia with the experimental drug or placebo; - 5 ml of venous blood was retained before, after, and 1 day after surgery for follow-up determination of serum associated factor levels; - To record their vital signs at any point during the anaesthetic process; Serum serological indexes related to oxidative stress and inflammation were determined. The agitation during the recovery period was recorded. The incidence and severity of ponv were recorded at 2h, 2-6h, and 6-24h postoperatively, and the use of palonosetron was also recorded.

NCT ID: NCT06237751 Not yet recruiting - Hepatectomy Clinical Trials

Preoperative Sildenafil Administration for Hepatectomy

Start date: January 31, 2024
Phase: N/A
Study type: Interventional

Laparoscopic Hepatectomy (LH) is an important treatment for liver diseases, and bleeding is one of the most common complications during dissection of the liver parenchyma. Control Low Central Venous Pressure (CLCVP) technique is currently one of the most important techniques to control intraoperative bleeding. It mainly consists of fluid restriction, position adjustment and use of vasodilators. However, these measures focus on decreasing CVP by reducing the volume of return blood, and less attention is paid to factors such as pulmonary vascular resistance and cardiac function. Sildenafil, known as Viagra, is currently used to treat erectile dysfunction and pulmonary hypertension in men. Its mechanism of action is to inhibit phosphodiesterase-5 (PDE-5) and increase cGMP levels leading to smooth muscle relaxation and vasodilation. Its pharmacological properties provide potential value for the treatment of many diseases. However, few studies have been conducted both domestically and internationally on the use of sildenafil citrate in LH related to CLCVP. The aim of this study is to investigate the following aspects: 1) the feasibility and effectiveness of sildenafil citrate applied to control low central venous pressure in LH, such as intraoperative bleeding, the impact of CVP, and the surgeon's operative field grading to assess the value of its clinical application; 2) the impact of sildenafil citrate applied to the function of the liver and important organs of the kidneys of the patients after LH surgery as well as the incidence of postoperative complications, and to assess the clinical application of its Safety.

NCT ID: NCT05669183 Recruiting - Cardiac Arrest Clinical Trials

Hemodynamic Comparison of Peripheral and Central VA ECMO.

RECOVERY
Start date: August 12, 2023
Phase:
Study type: Observational

The goal of this clinical trial is to monitor hemodynamic differences between central veno-arterial extracorporeal membrane oxygenation (VA ECMO) and peripheral VA ECMO. The main question it aims to answer is: - Efficacy of the different cannulation strategies for the establishment of for VA-ECMO circulation on hemodynamics and organ perfusion. Participants require VA ECMO support, will be divided into two groups in an intention-to-treat analysis: central artery cannulation and peripheral artery cannulation. Researchers will analyze different cannulation strategies for VA-ECMO and identify potential advantages and disadvantages for two groups of VA-ECMO.

NCT ID: NCT04491331 Completed - Prone Position Clinical Trials

Hemodynamic Changes Due to Prone Position

Start date: June 8, 2020
Phase:
Study type: Observational

Perioperative prone position may be associated with hemodynamic instability. The causes of instability have not yet been precisely elucidated. The aim of this study is to demonstrate physiological changes during prone positioning in healthy volunteers .

NCT ID: NCT03861364 Completed - Anesthesia, General Clinical Trials

Hemodynamics During Induction of General Anesthesia With High and Low Propofol Dose.

PH
Start date: September 3, 2019
Phase: Phase 4
Study type: Interventional

The study objective is to examine if a high propofol dose is non-inferior to a low dose in respect to hemodynamic stability in healthy patients during induction of general anesthesia with propofol and remifentanil.

NCT ID: NCT03401632 Completed - Critical Care Clinical Trials

Enteral Nutrition and Vasoactive Drugs

NUTRIVAD
Start date: January 15, 2017
Phase:
Study type: Observational

Enteral nutrition in critically ill patients undergoing vasoactive support due to hemodynamic instability is controversial. Hypothesis: enteral nutrition delivered in such patients can be feasible and safe.

NCT ID: NCT03128190 Completed - Clinical trials for Postoperative Complications

Multi-center Trial of Goal-directed Fluid Management Based on Pulse Pressure Variation Monitoring

GDTPPV
Start date: June 1, 2007
Phase: N/A
Study type: Interventional

Background: Intraoperative fluid therapy guided by mechanical ventilation-induced pulse-pressure variation (PPV) may improve outcomes after major surgery. It was tested this hypothesis in a multi-center study. Methods: The patients were included in two periods: a first control period (control group; n=147) in which intraoperative fluids were given according to clinical judgment. After a training period, intraoperative fluid management was titrated to maintain PPV< 10% in 109 surgical patients (PPV group). It was performed 1:1 propensity score matching to ensure the groups were comparable with regard to age, weight, duration of surgery, and type of operation. The primary endpoint was postoperative hospital length of stay.

NCT ID: NCT03027817 Completed - Clinical trials for Hemodynamics Instability

Cardiac Output and Other Hemodynamic Changes With Prone Position in Cervical Myelopathy Patients Undergoing Surgery

Start date: November 2014
Phase: N/A
Study type: Observational

Positioning a patient in prone position under anaesthesia significantly alters cardiovascular physiology. Cervical myelopathy patients are known to have autonomic dysfunction. Such patients when positioned in prone position under anaesthesia carry a higher risk of developing hemodynamic changes and this can compromise spinal cord perfusion. This prospective observational study was conducted on 30 patients with cervical myelopathy who underwent surgery in prone position at NIMHANS, Bangalore hospital. The non invasive cardiac output monitor (NICOM, Cheetah Medicals) was used to record various hemodynamic parameters. The hemodynamic parameters were recorded at baseline, post induction, post intubation, prior to prone position, post prone position, and every five minutes thereafter upto 20mins. The hemodynamic parameters that were recorded using the NICOM monitor: - HR - Heart rate (beats /min) - NIBP - non invasive blood pressure (mmHg) - MAP - mean arterial pressure(mmHg) - CO - cardiac output (l/min) - CI - cardiac index (l/min/m2) - SV - Stroke volume (ml/beat) - SVV -stroke volume variability (%) - TPR - total peripheral resistance (dynes. sec/cm5)