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Anesthesia clinical trials

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NCT ID: NCT05716399 Not yet recruiting - Anesthesia Clinical Trials

Effect of Acupoint Electrical Stimulation on Incidence of Hypotension After Spinal Anesthesia

Start date: February 20, 2023
Phase: N/A
Study type: Interventional

This study is intended to include elderly patients who are selected to undergo lower limb and pelvic orthopedic surgery under spinal anesthesia. Through prospective, randomized and controlled clinical trials, the investigators will observe the effect of this treatment on the incidence of hypotension in elderly patients after spinal anesthesia through TEAS points Neiguan and Quchi before or during surgery, and further explore its related mechanisms.

NCT ID: NCT05709041 Not yet recruiting - Obesity Clinical Trials

Effect of Transpulmonary Pressure Guided Ventilation on Intraoperative Right Heart Function

Start date: January 30, 2023
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to determine whether different types of ventilator settings during surgery change the relationship between the pressures in the lungs and the function of the heart. In this study, patients will be randomly assigned (like flipping a coin) to receive either standard or individualized (research) lung protective ventilator settings. Before surgery, patients will be given an 8-item verbal questionnaire about any respiratory symptoms. After patients are asleep for surgery, an ultrasound probe will be inserted into the esophagus (food pipe) and stomach to examine the heart and lungs and take ultrasound pictures. The ultrasound probe is then removed. Next, a small balloon catheter (a narrow tube smaller in diameter than a pencil lead) will be placed in the esophagus, where it will be used to measure the pressures in the chest and lungs. For patients who are assigned to standard ventilator settings, the ventilator settings and pressures during surgery will be recorded. For patients assigned to individualized (research) ventilator settings, the pressures from the balloon catheter will be used to adjust the ventilator settings every 30 minutes during surgery. A second ultrasound pictures of the heart and lungs will be obtained at the point at which the patient is placed into the Trendelenburg position. At the end of surgery and before the patient is awake, the balloon catheter will be removed, the ultrasound probe will be inserted, a third set of ultrasound pictures of the heart and lungs will be obtained, and the ultrasound probe then removed. Patients will be telephoned 30 days after surgery to ask about their recovery. The 8-item respiratory symptom questionnaire will be repeated at this time.

NCT ID: NCT05706337 Not yet recruiting - Pain Clinical Trials

Clinical Observation of Ciprofol for Anesthesia Induction

Start date: February 1, 2023
Phase: Phase 4
Study type: Interventional

To evaluate the effect of ciprofol anesthesia Induction on hemodynamics in elderly patients undergoing elective noncardiac surgery,a prospective, randomized, controlled trial.

NCT ID: NCT05662163 Not yet recruiting - Anesthesia Clinical Trials

Effect of General Anesthesia Method on Cardiac Risk Patients on Ischemia Modified Markers

Start date: December 30, 2022
Phase: N/A
Study type: Interventional

To examine the effects of the general anesthesia method chosen in non-cardiac surgical operations of patients with cardiac risk on the levels of cardiac markers

NCT ID: NCT05626153 Not yet recruiting - Anesthesia Clinical Trials

Anesthesia Quality Improvement and Patients With Planned ICU Admission

Start date: December 2022
Phase: N/A
Study type: Interventional

Intensive care unit (ICU) is an important part of perioperative management for high-risk patients but is associated with higher medical costs. Improper ICU admission may produce overtreatment without beneficial effects. In clinical practice, delayed recovery after general anesthesia is a common indication for ICU admission after surgery. The concept of Enhanced Recovery After Surgery recommends early extubation. The investigators suppose that, for patients with planned ICU admission after elective surgery, implementing anesthesia quality improvement including extubation in the operating room will reduce the rate of ICU admission after surgery without increasing complications.

NCT ID: NCT05619627 Not yet recruiting - Anesthesia Clinical Trials

Oral Dexmedetomidine in Pediatric MRI

Start date: April 1, 2024
Phase: Phase 1
Study type: Interventional

The objective of this preliminary study is to assess the utility of oral dexmedetomidine as the sole sedative agent in pediatric population undergoing MRI

NCT ID: NCT05601622 Not yet recruiting - Anesthesia Clinical Trials

RPVI for Fluid Responsiveness in Children

Start date: November 15, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to validate Rainbow pleth variability index for prediction of fluid responsiveness in children.

NCT ID: NCT05566067 Not yet recruiting - Anesthesia Clinical Trials

Survey of Anesthesiology Residents' Perceptions of Critical Care Medicine as a Career

Start date: December 2023
Phase:
Study type: Observational

This study's goal is to investigate the reasons behind the decline in interest in critical care fellowships among anesthesia residents.

NCT ID: NCT05564741 Not yet recruiting - Anesthesia Clinical Trials

Acute Hip Fracture and Spinal Anaesthesia Injection Time

Start date: October 2022
Phase: Phase 4
Study type: Interventional

The systemic effects of spinal anesthesia is not fully known. Our aim of this study is to assess whether there is a difference in hemodynamic effects if the spinal dose is given fast (15s) or slow (90s) in elderly patients with acute hip fracture (AHF). Ninety (n=90) patients with AHF planned for surgery within 72h at our hospital will be enrolled in the study and randomly devided into two groups. The patients will receive one predetermined dose of spinal anesthesia followed by an advanced minimally-invasive hemodynamic monitoring through an arterial line using FloTrac-system. The hemodynamic parameters will be conducted 10 minutes prior to the spinal anaesthesia and 30 minutes after the spinal block is given. Hypotension was defined as a fall in MAP > 30 % or a MAP <65mmHg.

NCT ID: NCT05525351 Not yet recruiting - Anesthesia Clinical Trials

The Application and Validation of Triple Drug Response Surface Models on Density Spectral Array in Clinical Anesthesia

Start date: October 2022
Phase:
Study type: Observational

Precision anesthesia is the current trend. The benefits including faster recovery, earlier return to normal activity, increased patient satisfaction and shorter length of stay. In order to avoid unnecessarily deep or too light anesthesia, processed electroencephalogram (EEG) monitors are applied for accurate assessment of the depth of anesthesia (DoA). Bispectral index (BIS) and PSI monitor are among the most widely used. Recently, density spectral array (DSA) has been developed to facilitate the interpretation of EEG signals. Real-time DSA EEG monitoring helps in detecting even subtle changes in the depth of anesthesia and provides more comprehensive information then simple digits. An emerging field of pharmacodynamics in anesthesia is the response surface models. They describe the interaction of different anesthetics during sedation or anesthesia. Our research team has developed the first comprehensive two-drug response surface models for midazolam and alfentanil during gastrointestinal procedural sedations. However, adequate anesthesia is often achieved with multiple drugs. Two-drug models thus have limited applications. We aim to extend the models into three-drug interactions where it can be used for a broader range of clinical scenarios. The main goal of the study is to establish and validate the three-drug response surface model by collecting and analyzing EEG parameters (BIS or PSI values, DSA, SEF95 (95% spectral edge frequency) and MF (Median frequency) ) from 60 patients undergoing general anesthesia for thoracic surgeries. We aim to establish the models that help anesthesiologist to achieve rapid emergence, appropriate analgesia, adequate DoA, and patient safety. The secondary aim is to apply this model to provide a guideline for drug dosage adjustment and improve the quality of anesthesia.