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Lung Transplantation clinical trials

View clinical trials related to Lung Transplantation.

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NCT ID: NCT05689476 Recruiting - Clinical trials for Lung Transplantation

Electrical Activity of the Diaphragm and Respiratory Mechanics During NAVA

NAVAMECH
Start date: December 27, 2022
Phase: N/A
Study type: Interventional

Protective ventilatory strategy should be applied to reduce both ventilator-induced lung injury (VILI) and ventilator-induced diaphragm dysfunction (VIDD) after Lung Transplantation (LTx). Neurally Adjusted Ventilatory Assist (NAVA) is an assisted ventilation mode in which respiratory support is coordinated by the electrical activity of the diaphragm (EAdi). Aim of the study is to assess the physiological relationship between neural respiratory drive as assessed by EAdi and tidal volume, driving pressure and mechanical power, at different levels of ventilatory assist, in the absence of pulmonary vagal afferent feedback.

NCT ID: NCT05410522 Recruiting - Clinical trials for Lung Transplantation

Electrostimulation Program for Lung Transplant Recipients in the ICU

Start date: May 9, 2022
Phase: N/A
Study type: Interventional

This study aims to evaluate rectus femoris muscle mass in lung transplant recipients and the effect of a training program during ICU admission based on the use of electrical muscle stimulation (EMS)

NCT ID: NCT05309551 Recruiting - Rehabilitation Clinical Trials

Inspiratory Muscle Training Immediately After Lung Transplantation

Start date: April 20, 2022
Phase: N/A
Study type: Interventional

Following lung transplantation (LTX), patients may exhibit respiratory and skeletal muscle weakness that will affect exercise capacity, increase dyspnea and fatigue, limit activities of daily living (ADL) and decrease quality of life. Inspiratory muscle training (IMT) has been extensively studied in a variety of non-LTX populations and research has shown that IMT improves exercise capacity, diaphragmatic thickness, and reduced dyspnea during activities of daily living and improved quality of life in patients with advanced lung disease. The aim of this randomized controlled study is to investigate the benefits of providing inspiratory muscle training via use of an inspiratory muscle trainer device in addition to standard physical therapy in the acute phase of rehabilitation following LTX. Patients targeted for enrollment will be those with any type of advanced lung disease requiring LTX with the objective of demonstrating improvements in respiratory muscle recovery, perceived dyspnea, severity of fatigue, and overall functional status following the transplant procedure.

NCT ID: NCT04891094 Completed - Clinical trials for Lung Transplantation

Lung and Diaphragm Ultrasound in the Early Postoperative Course Following Lung Transplantation

LUS
Start date: April 16, 2021
Phase: N/A
Study type: Interventional

This feasibility study tries to define the value of daily Lung and Diaphragm Ultrasound in the early postoperative course following Lung transplantation by comparing its diagnostic accuracy with that of standard of care diagnostic procedures

NCT ID: NCT04667806 Not yet recruiting - Clinical trials for Lung Transplantation

Health Related Quality of Life in Lung Transplantation in Strasbourg

Start date: April 2021
Phase:
Study type: Observational

The aim of this study is to study the quality of life in lung transplant patients. The cohort includes all of the surviving and transplanted patients at the New Civil Hospital in Strasbourg between 2008 and 2018. The main objective is to assess the quality of life of this cohort by two questionnaires which are the SF36 (generic score) and the saint Georges's questionnaire (specific score). The secondary objectives are the measurement of survival after lung transplantation, the comparison of the quality of life of these patients with that of the general population by the SF36 questionnaire, the search for perioperative factors influencing the quality of life and finally the search for an association between quality of life and socio-professional life.

NCT ID: NCT04616365 Completed - Clinical trials for Lung Transplantation

Planned Semi-Elective Lung Tx Study

Start date: August 26, 2020
Phase: N/A
Study type: Interventional

In the current practice of lung transplantation, transplants are performed on a 24/7 schedule with a significant amount of procedures occurring overnight in order to minimize organ ischemic time. However, transplantation during the day time may lead to several advantages related to patient safety, including the presence of rested staff performing optimally, larger number of in-house professionals for emergency situations, and professional well-being. Advances and refinements in preservation practices have evolved to show that extended periods of preservation can be achieved without compromising outcome. Based on this, it is hypothesized that the avoidance of nighttime lung transplantation through prolonged pulmonary preservation will lead to at least similar patient outcomes compared to the current practice of 24/7 transplantation. During the period of this study, overnight transplants will be moved to a later start time (earliest 6AM). If lungs meet criteria for direct transplantation, they will be preserved with cold static preservation at 10°C within a special refrigerator. The maximum preservation time from donor cold flush to recipient anesthesia start time will be 12 hours.

NCT ID: NCT04244305 Active, not recruiting - Clinical trials for Lung Transplantation

Endurance Training in Patients Undergoing Lung Transplantation

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

Lung Transplantation is usually the last option for patients with chronic respiratory conditions in the late stages of the disease. Pulmonary rehabilitation and, particularly, endurance training, is a cornerstone in the management of these patients both during the pre-operative as well as the post-operative period as it improves cardiopulmonary fitness, muscle mass, muscle strength, health-related quality of life and potentially, survival. However, very few studies have been published addressing which modality of training, intensity, frequency or duration of training provides the best possible results in these patients. Therefore, the objective of this study was to compare two training modalities (treadmill walking versus cycle-ergometry) on functional capacity, muscle strength and lung function.

NCT ID: NCT04122768 Completed - Clinical trials for Lung Transplantation

Activity Coaching in Patients Post Lung Transplantation

Start date: November 6, 2019
Phase: N/A
Study type: Interventional

Lung transplantation is an ultimate, effective treatment option for selected patients with end stage lung disease, improving quality of life and extending survival. Because of the improved survival during the last decades, enhancing the long term condition after lung transplantation has now become a focus for disease management. The co-presence of non-communicable diseases is common and poses new challenges to disease management. These comorbidities have been related to physical activity in the healthy population. As in other chronic respiratory disease, physical inactivity is a common feature of patients after LTX. Despite near normal lung function, exercise intolerance and physical inactivity persist up to years after the transplantation. Literature on effective interventions to increase physical activity are scarce in this population. Therefore, the present project aims to test the effectiveness of a tele coaching program to enhance physical activity and to analyze the association between physical activity and long-term health benefits in this population at risk. These research questions will be answered based on a randomized controlled trial. Patients that are active at baseline will be followed up in a cohort study.

NCT ID: NCT04016194 Completed - Cystic Fibrosis Clinical Trials

Prediction of Survival in Children With Cystic Fibrosis Using the Multiple-breath Washout

Start date: January 1, 1990
Phase:
Study type: Observational

Retrospective cohort study using routinely collected annual data on lung clearance index (LCI) in combination with clinical data to predict survival in patients with Cystic Fibrosis. The primary study endpoint is the association of LCI with the compound outcome survival or lung transplantation in patients with CF.

NCT ID: NCT03970265 Completed - Clinical trials for Lung Transplantation

Development a Method to Extract Antibiotic Concentration From Interstitial Lung and Epithelial Lining Fluid.

ALF
Start date: August 15, 2019
Phase:
Study type: Observational

Infections are critical factors for the survival of critically ill patients. A serious problem is the high variability of antibiotic concentrations in critically ill patients. This may result in the risk of underdosage with possible ineffective therapeutic levels as well as in the risk of overdosage with possible adverse and toxic effects. Essential for the effectiveness of antibiotic therapy is the antibiotic concentration at target site. The goal of this study is to establish a method to extract Interstitial Lung Fluid (ILF) and Epithelial Lining Fluid (ELF) for antibiotic concentration measurements in patients following lung Transplantation and to calculate a tissue/serum concentration ratio. Improved knowledge regarding tissue penetration of Antibiotics may help to optimize drug dosing and management.