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Anesthesia clinical trials

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NCT ID: NCT04151264 Active, not recruiting - Anesthesia Clinical Trials

Influence of the "Hypotension Probability Index" on Intraoperative and Postoperative Hypotension in ENT- and OM-Surgery

Start date: May 30, 2020
Phase: N/A
Study type: Interventional

The aim of the project is to investigate whether the use of the HPI can reduce the number and duration of intra- and postoperative hypotension in ventilated patients during and two hours after extensive surgery in the head and neck area compared to the established monitoring.

NCT ID: NCT04149314 Completed - Anesthesia Clinical Trials

The "Hypotension Prediction Index" in Patients Undergoing Lung Surgery

Start date: November 20, 2019
Phase: N/A
Study type: Interventional

The "Hypotension Prediction Index (HPI)" was established by the Edwards Lifescience Company (Irvine, California, USA) and is CE certified. As part of the Edwards Acumen Decision-Support-Software-Suite the HPI is supported by the minimal invasive FloTrac Sensor. The HPI displays the probability of an occurring hypotension. The software was established with the help of 20.000 analyzed patient events. If the upper limit of the HPI is reached, the software is alarming the treating physician 8. At the university hospital of Giessen HPI analyses are used in the daily clinical routine as well as for scientific purposes. Preliminary data of the HPI-I-Trial ("Influence of the Hypotension Prediction Index on the number and duration of intraoperative hypotension in primary hip-endoprothetic replacement", University Hospital of Giessen) included patients, which underwent hip-endoprothetic replacement surgery and revealed that the use of HPI with a goal directed therapy (GDT) protocol compared to standard care significantly reduced the incidence and duration of intraoperative hypotension. Therefore HPI with GDT might reduce the incidence of hypotension related complications in a sicker patient cohort. The aim of the study is to investigate whether a goal directed treatment according to the Hypotension Prediction Index compared to standard care can reduce the incidence of intraoperative hypotension in patients under single lung ventilation.

NCT ID: NCT04146233 Completed - Anesthesia Clinical Trials

POCUS Analysis of the Gastric Emptying Time of Orange Juice With and Without Pulp

Start date: November 19, 2019
Phase: N/A
Study type: Interventional

Preoperative fasting guidelines for anesthesia recommend waiting two hours after ingesting a clear liquid and six hours after ingesting a light meal. Due to the presence of pulp, orange juice is considered a light meal by current guidelines which means a patient must wait six hours before undergoing general anesthesia. This study will use ultrasound of stomach of healthy volunteers to determine if the presence of pulp actually increases the transit time for orange juice.

NCT ID: NCT04145752 Completed - Anesthesia Clinical Trials

Nurse Led Ultrasound Guided Femoral Nerve Block in the Emergency Department

URGENT
Start date: February 11, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effects of task shifting from anesthesiologists to special trained nurses performing femoral nerve block (FNB) in patients with hip fracture in the emergency department (ED) at Vestfold Hospital Trust (VHT). A sample of nurses (n= 6) will perform ultrasound guided FNB in hip fracture patients (n=25) admitted to the ED at VHT. This cohort will be compared to another cohort of hip fracture patients (n=25). This cohort will follow standard of care where the femoral nerve block is often performed by anesthesiologists. The study is a prospective, controlled randomized trial.

NCT ID: NCT04145583 Completed - Anesthesia Clinical Trials

A Study Evaluating Drug-Drug Interaction (DDI) Between HSK3486 Injectable Emulsion and Voriconazole Tablets

Start date: December 14, 2019
Phase: Phase 1
Study type: Interventional

This is a single-center, open-label, randomized, two-stage, two-way crossover study evaluating the effect of voriconazole on the PK, PD, and safety of HSK3486 in healthy subjects.

NCT ID: NCT04144933 Recruiting - Anesthesia Clinical Trials

Effect of Multimodal Opioid-free Anesthesia on Return of Bowel Function in Laparoscopic Colorectal Surgery

RUMBLE
Start date: May 15, 2021
Phase: Phase 3
Study type: Interventional

The objective of this study is to determine if an opioid-free general anesthetic (OFA) technique utilizing lidocaine, ketamine, dexmedetomidine and magnesium reduce postoperative opioid consumption and speed return of bowel function in patients undergoing elective, laparoscopic, colorectal surgery compared to traditional opioid-containing general anesthetic techniques. It is hypothesized that this intraoperative OFA regimen will reduce postoperative opioid consumption, and expedite return of bowel function in this population.

NCT ID: NCT04144803 Active, not recruiting - Anesthesia Clinical Trials

Brain Oxygenation During Prehospital Anesthesia: an Observational Study

BOPRA
Start date: November 18, 2019
Phase:
Study type: Observational

Brain oxygenation of adult patients undergoing prehospital emergency anesthesia is monitored using noninvasive near-infrared spectroscopy. Patients are afterwards interviewed to define neurological outcome to measure quality of life. The purpose of this study is to reveal the risk factors of prehospital anesthesia related cerebral desaturation events (CDE) and to define the association between CDE and survival, neurological outcome or quality of life.

NCT ID: NCT04138966 Recruiting - Anesthesia Clinical Trials

Comparing Skin Conductance and Nol-index

Start date: October 20, 2019
Phase:
Study type: Observational

Comparison of twà different nociception monitors during general anesthesia

NCT ID: NCT04136210 Recruiting - Anesthesia Clinical Trials

Registry Construction for Perioperative Data in Patients Undergoing Cardiovascular Surgery

Start date: September 19, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this registry is to obtain perioperative data in patients undergoing cardiac or thoracic aortic surgery and find out relations between the data and investigate several causes affecting postoperative complications.

NCT ID: NCT04135651 Completed - Anesthesia Clinical Trials

Paratracheal Esophagus Pressure on the Intubation With Pentax Airway Scope

Start date: December 9, 2019
Phase: N/A
Study type: Interventional

Recently, left paratracheal pressure was introduced as an alternative method to prevent pulmonary aspiration instead of cricoid pressure. Criocoid pressure is known to worsen glottic visibility when using Pentax.However, the effects of left paratracheal pressure on glottic view when using Pentax are not studied yet. In this study, the subjects are divided into two groups (group I: left paratracheal pressure applied before intubation, group II: conventional cricoid pressure applied before intubation). Investigators will assess the glottic view during intubation using Pentax.