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ICU Acquired Weakness clinical trials

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NCT ID: NCT04922814 Not yet recruiting - Clinical trials for COVID-19 Acute Respiratory Distress Syndrome

Comparison for the Effect of Neuromuscular Blocking Agents Versus Sedation Alone on Severe ARDS Patients Due to COVID-19

Start date: August 1, 2021
Phase: N/A
Study type: Interventional

Many questions about management of COVID-19 are still not answered. So, we recruit this study aiming to evaluate improvement of oxygenation in COVID-19 patients with severe ARDS, to improve morbidity and mortality of ICU covid patients, to participate in understanding of real hidden pathophysiology of COVID-19.

NCT ID: NCT04914065 Completed - Quality of Life Clinical Trials

Predictors of Prognosis in Patients With Critical Illness.

Start date: January 1, 2020
Phase:
Study type: Observational

Recently, intensive care unit acquired weakness (ICUAW) has become a hotspot issue in the patients with critical illness. The symptoms of ICUAW, including sensory impairment and muscle atrophy, may lead to poor quality of life even though the patients discharged from the ICU for a long time. Therefore, an ounce of prevention is worth a pound of cure. At the same time, early evaluation is necessary to keep critically ill patients away from ICUAW. Medical Research Council (MRC) scale is the most common approach for diagnosis clinically. Regarding the interrater variation of MRC, handgrip strength (HGS) has been thought to be a simple and accurate alternative. However, HGS does not belong to antigravity or respiratory muscle which are the first to be affected by immobilization. It is still unknown whether HGS can represent the general muscle condition in ICU or not. Additionally, previous studies have proved that patients with critical illness in the ICU would have better prognosis and less complications, if they undergo physical therapy as soon as possible. In addition to early ventilator weaning and reduced mortality rate, physical therapy could enhance quality of life (QoL) after patient discharges from hospital. However, early mobility in the ICU mainly emphasizes cardiopulmonary patients due to the traditional concept in Taiwan. Hence, the duration of mechanical ventilation in the critical patients will affect the timing to receive physical therapy, even impact the improvement of QoL. Because of these reasons, this study will investigate the relationship between HGS and muscle mass among patients with critical illness and find the predictors of the short-term and long-term goals in the ICU, including ventilator weaning and QoL after hospital discharge.

NCT ID: NCT04811638 Completed - Clinical trials for ICU Acquired Weakness

The Validity and Reliability Study of the Chelsea Critical Care Physical Assesment Tool

Start date: January 11, 2021
Phase:
Study type: Observational

This study is aimed at providing an translation and cross-cultural adaptation of Chelsea Critical Care Physical Assesment Tool (CPAx) and tested its reliability and validity.

NCT ID: NCT04810273 Completed - Trauma Clinical Trials

Effect of Progressive Early Mobilization in Patients With TBI

Start date: March 30, 2021
Phase: N/A
Study type: Interventional

traumatic brain injury (TBI) is a major public health concern worldwide. Patients with moderate-severe TBI have high rates of disability at the acute phase and frequently require protracted rehabilitation with prolonged periods of recovery. Recently, it has been found that the use of progressive early mobilization (EM) protocols for critical trauma patients may minimize the functional declines during intensive care unit (ICU) stays. However, prior early mobilization studies have found that the survivors of moderate-severe TBI often experience a greater incidence of neurological injuries with other organ injury than other critical care patients. No randomized controlled trials thus far have utilized measure the influence or effect of early progressive EM protocols on the functional recovery of moderate-severe TBI patients.

NCT ID: NCT04722445 Completed - Clinical trials for ICU Acquired Weakness

Ultrasound Measurement of Quadriceps Shortening During Neuromuscular Electrical Stimulation in Critically Ill Patients

DETECT
Start date: August 16, 2021
Phase:
Study type: Observational

ICU-Aw is highly prevalent (50%) among critically ill patients. Its diagnosis is usually delayed as it requires patients' awakening and collaboration to provide accurate measurement. This study aims to investigate the accuracy of an early ultrasound measurement of quadriceps shortening during neuromuscular electrical stimulation to diagnose future ICU-Aw in critically ill patients.

NCT ID: NCT04647539 Completed - Fungal Infection Clinical Trials

Emerging Invasive Fungal Infections in Critically Ill Patients

EIFI
Start date: January 1, 2006
Phase:
Study type: Observational

Rationale: Beside Candida and Aspergillus, emerging invasive fungal infections (EIFIs) are increasing in intensive care setting and are associated with high morbidity and mortality. However, data are scarce, particularly in ICU settings and for EIFIs other than mucormycosis. Objectives: to describe epidemiological trends and clinical features of EIFIs in intensive care units (ICU) and to assess their outcome. Methods: All records of adult patients diagnosed with an EIFI in a medical ICU between 2006 and 2019 were analyzed retrospectively. In-ICU mortality was assessed, then factors associated with mortality were identified. Survival at day-90 was calculated by the Kaplan-Meier method.

NCT ID: NCT04565002 Recruiting - Clinical trials for ICU Acquired Weakness

Transcutaneous Electrical Diaphragmatic Stimulation in Critically Ill Elderly Patients

Start date: June 25, 2018
Phase: N/A
Study type: Interventional

Abstract..................................................................................... .....................04 Introduction................................................................................. ...................10 Methods...................................................................................... ...................14 Financial Support...................................................................................... .....22 References................................................................................... ..................24

NCT ID: NCT04430283 Terminated - Clinical trials for ICU Acquired Weakness

Evaluation of FDY-5301 in Major Trauma Patients in ICU

Start date: September 20, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics (PK) of FDY-5301 compared to placebo in major trauma ICU patients at risk of intensive care unit acquired weakness (ICUAW)

NCT ID: NCT04396197 Completed - COVID-19 Clinical Trials

Physical Activity Levels in COVID-19 Patients Admitted to Intensive Care

Start date: March 1, 2020
Phase:
Study type: Observational

This is an observational study exploring the levels of mobility and rehabilitation in patients admitted to critical care with a confirmed diagnosis of COVID-19

NCT ID: NCT04373811 Active, not recruiting - COVID-19 Clinical Trials

One-Year Quality of Life and Functional Prognosis of COVID-19 Patients in Post-ICU Setting

COVENTRY
Start date: April 16, 2020
Phase:
Study type: Observational

The COVID-19 disease has been subject to numerous publications since its emergence. Almost 20% of people suffering from COVID-19 develop severe to critical symptoms and require hospitalization, often in Intensive Care Unit (ICU). Respiratory failure is the main reason for admission in ICU of these patients. Therapeutic strategies implemented for the management of critically-ill patients may often lead to short-term muscular and functional alterations resulting in ICU-Acquired Weakness (ICUAW). These lead to long-term disabilities expressing trough dependence and quality of life impairment of survivors. The purpose of this study is to assess the quality of life, dependence and survival at one year in patients who survived from COVID-19 in ICU and are admitted in post-ICU setting for difficult weaning purpose. Ancillary studies aim to assess the course of muscle function (atrophy, structural modifications), lung function (loss of aeration) and safety of early mobilization.