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Critical Care clinical trials

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NCT ID: NCT05399927 Completed - Clinical trials for Cardiovascular Diseases

Music as Intervention Nursing in Ambulances

Start date: July 2015
Phase: N/A
Study type: Interventional

Background: Patients with acute cardiovascular disease require out-of-hospital care during the most critical and vulnerable periods of their illness. Objectives: To evaluate the influence of music intervention in patients with an acute cardiovascular condition during their transfer in Advanced Life Support (ALS) ambulances. Method: A controlled, randomized experimental analytical study of cases and controls. The intervention group was exposed to relaxing music with sounds from nature. Data related to demographic factors, comorbidities, clinical constants, and drugs administered were gathered. The qualitative variables were summarized using counts and percentages, and the quantitative variables through means and standard deviations.

NCT ID: NCT05386303 Not yet recruiting - Critical Care Clinical Trials

Quantitative Pupillometry

HYDRO-NiP
Start date: May 31, 2022
Phase:
Study type: Observational

The aim of this study is to assess the diagnostic ability of quantitative pupillometry for the early detection of hydrocephalus during the weaning process of the external ventricular drain.

NCT ID: NCT05380687 Recruiting - Respiratory Failure Clinical Trials

Time Course of Neuro-ventilatory Efficiency During a Spontaneous Breathing Training

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

The TONES trial aims to evaluate the neuroventilatory efficiency (NVE = tidal volume / peak voltage of diaphragm contraction) measured during a zero-assist manoeuvre (ZAM, i.e. with PEEP but without pressure support). This novel parameter, NVE-ZAM, will be studied in a blocked, crossover, repeated measures design. Possible confounders, such as activity of respiratory muscles other than the diaphragm, are included. The investigators hypothesized that - the NVE during a zero-assist maneuver has a low variability and high repeatability at the same level of PEEP (within subjects, within blocks) - NVE-ZAM trends differ between participants (between subjects, within blocks) and between PEEP levels (within subjects, between blocks) The primary aim is to study the variability and repeatability of the NVE-ZAM within subjects and within blocks. Additionally, the effect of PEEP, muscle fatigue and recruitment of the accessory and expiratory muscles of respiration on the NVE-ZAM will be studied in an exploratory analysis (in multiple combinations of within and between subjects and/or blocks).

NCT ID: NCT05295862 Recruiting - Stroke, Acute Clinical Trials

Giessen Stroke Registry

GIST
Start date: November 30, 2023
Phase:
Study type: Observational [Patient Registry]

The aim of the planned study project is to assess the current situation regarding the treatment of patients with stroke. Specifically, various treatment strategies are to be associated and correlated with clinical endpoints, mortality or functional outcome in order to generate arguments for or against individual aspects of therapy. The focus will be on unresolved treatment approaches in acute therapy (e.g. periprocedural management, such as blood pressure, blood glucose, temperature, or airway management, during recanalizing therapies) as well as in secondary prevention on the stroke unit or intensive care unit, such as starting point, mode, and dosage of antithrombotic therapies.

NCT ID: NCT05281224 Completed - Critical Care Clinical Trials

Ventilator Tube Holder for Patients With a Tracheostomy

TRACHVest
Start date: October 21, 2021
Phase:
Study type: Observational

Patients admitted to the critical care unit (CCU) at University Hospital Wales (UHW) have a variety of life-threatening conditions which require specialist care, often including a period of sedation and mechanical ventilation. As a consequence of critical illness, survivors often experience multiple sequela, including muscle weakness which leads to reduced mobility and physical function, especially if they experience a prolonged stay within critical care. Patients who require mechanical ventilation (MV) usually initially receive this via an endotracheal tube (ETT), but if the need for MV continues then this support is delivered through a tracheostomy tube. A small opening is made in the front of the patient's neck and the tracheostomy tube inserted into the trachea. This is connected to the ventilator and allows ventilatory support to be delivered without the need for an ETT. Consequently, sedation levels can be reduced, facilitating improved patient comfort, communication, eating, drinking and mobilisation. Early rehabilitation is a key component of a patient's critical care journey and patients are supported with this by a number of specialist staff including physiotherapists, occupational therapists, nurses and support workers. Part of this rehabilitation may include helping a patient to sit on the edge of the bed, stand and mobilise. During rehabilitation sessions and other aspects of patient care, safety is paramount and staff must take care to ensure all lines and attachments are not dislodged. This includes tubing connecting the ventilator to the tracheostomy, excessive movement of which can cause damage to the airway, breakdown of skin and partial or complete dislodgement requiring immediate intervention. The number of staff required to help mobilise a patient and maintain safety can be significant, especially when the patient has several attachments. Unfortunately, this staffing burden may contribute to reduced levels of patient mobilization and rehabilitation. However, it is possible that specially designed equipment may facilitate patient mobilization with increased safety and reduced resource requirements. This study will test a garment that may achieve this and obtain staff and patient opinion on its utility.

NCT ID: NCT05272267 Completed - Critical Care Clinical Trials

Transforming ED Throughput With AI-Driven Clinical Decision Support System

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

The aims of this study is to integrate real-time data flow infrastructure between hospital information system and AI models and to conduct a cluster randomized crossover trial to evaluate the efficacy of the AI models in improving patient flow and relieving ED crowding.

NCT ID: NCT05260710 Not yet recruiting - Telemedicine Clinical Trials

Evaluation of the Impact of Telemedicine in Pediatric Intensive Care Units

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

This study will be a cluster randomized controlled trial to assess the impact of telemedicine in Pediatric Intensive Care Units (PICU), through daily tele-rounds with a board certified physician and educational activities, in improving clinical-assistance indicators, as well as reducing the length of stay in the PICU.

NCT ID: NCT05255783 Recruiting - Critical Care Clinical Trials

The Performance of Dexcom G6 Glucose Monitoring in Critically Ill Patients

Start date: November 19, 2021
Phase: N/A
Study type: Interventional

This is an investigator-initiated, prospective, observational accuracy-study. The aim of the study is to test the feasibility, safety, and accuracy of a subcutaneous continuous glucose monitoring system (the Dexcom G6 glucose monitoring system) in critically ill patients. A total of 40 adult patients admitted to the intensive care unit requiring intravenous insulin infusion to maintain blood glucose within target range will be enrolled. Subcutaneous glucose readings will be compared with routine arterial blood glucose measurements to determine accuracy.

NCT ID: NCT05205525 Completed - Critical Care Clinical Trials

Delayed Antibiotic Therapy in Non-severe Ventilator Acquired Pneumonia (VAP)

DELAVAP
Start date: January 6, 2022
Phase:
Study type: Observational

This retro-prospective monocentric observational study compare the impact of the implementation of a restrictive (delayed) versus aggressive (immediate) antibiotic strategy for Ventilator Acquired Pneumonia suspicion without severity symptoms.

NCT ID: NCT05196997 Completed - Critical Care Clinical Trials

The De-Morton Mobility Index Turkish Version in Intensive Care Patients

Start date: April 1, 2018
Phase:
Study type: Observational [Patient Registry]

De Morton Mobility Index is recommended for the evaluation of mobility in the evidence-based guidelines, in patients in intensive care units. The aim of our study is to examine the validity and reliability of the Turkish version of the De Morton Mobility Index in patients hospitalized in the respiratory intensive care unit.