Clinical Trials for Respiratory Failure

Currently registered clinical trials for Respiratory Failure from ClinicalTrials.gov. 20 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Respiratory Failure from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 20
  • Active, not recruiting: 3
  • Completed: 13
  • Other: 14

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT05446272 — The Diaphragmatic Initiated Ventilatory Assist (DIVA) Trial

StatusRecruiting
PhaseN/A
SponsorUniversity of Pennsylvania
Enrollment478
Study TypeINTERVENTIONAL
ConditionsExtubation Failure; Bronchopulmonary Dysplasia; Death
Interventions;

DIVA is a pragmatic randomized clinical trial (RCT) to determine: among (P) preterm infants born 23 0/7-28 6/7 weeks gestation undergoing extubation from mechanical ventilation, whether (I) Non-invasive neurally adjusted ventilatory assist (NIV-NAVA) (C) compared with Non-synchronized nasal intermittent positive pressure ventilation (NS-NIPPV), will reduce the incidence of (O) extubation failur…

NCT06066502 — Precision Ventilation vs Standard Care for Acute Respiratory Distress Syndrome

StatusRecruiting
PhasePhase 3
SponsorBeth Israel Deaconess Medical Center
Enrollment1100
Study TypeINTERVENTIONAL
ConditionsAcute Respiratory Distress Syndrome; Respiratory Failure
Interventions;

The goal of this interventional study is to compare standard mechanical ventilation to a lung-stress oriented ventilation strategy in patients with Acute Respiratory Distress Syndrome (ARDS). Participants will be ventilated according to one of two different strategies. The main question the study hopes to answer is whether the personalized ventilation strategy helps improve survival.

NCT06446453 — Echography-guided Surfactant THERapy (ESTHER) For Preterm Infants With Respiratory Failure

StatusRecruiting
PhaseN/A
SponsorConnecticut Children’s Medical Center
Enrollment52
Study TypeINTERVENTIONAL
ConditionsRespiratory Distress Syndrome, Newborn; Pulmonary Surfactants; Intensive Care Units, Neonatal
Interventions

Point-of-care ultrasound (POCUS) is the use of ultrasound by the bedside provider in real time to answer a specific question and guide medical management. POCUS can be used to diagnose the severity of neonatal respiratory distress syndrome (RDS) through a lung ultrasound score. Lung ultrasound scores have also been shown to predict if an infant is treated with an initial dose of surfactant. The…

NCT05756387 — Improving Chronic Nocturnal Noninvasive Ventilation: a Multimodality Approach

StatusRecruiting
PhaseN/A
SponsorUniversity Medical Center Groningen
Enrollment100
Study TypeOBSERVATIONAL
ConditionsChronic Respiratory Failure; Non-invasive Ventilation
Interventions

The aim of the data collection is to create an advanced reliable method to remotely monitor patient on chronic home non-invasive ventilation (NIV), both regarding ventilatory efficacy and patient comfort, both in the hospital and at home by assessing gas exchange, lung mechanics and the interaction between the patient and the ventilator.

For this purpose, we will set-up of databank of synchron…

NCT06927986 — Phase III Trial of SYS6010 Versus Platinum-based Chemotherapy for EGFR-mutated NSCLC(SYNSTAR01)

StatusRecruiting
PhasePhase 3
SponsorCSPC Megalith Biopharmaceutical Co.,Ltd.
Enrollment380
Study TypeINTERVENTIONAL
ConditionsEGFR-mutated Locally Advanced or Metastatic NSCLC
Interventions; ;

To evaluate the efficacy and safety of SYS6010 versus platinum-based chemotherapy in participants with EGFR-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC)

NCT06832306 — STimulation to Activate RespIration

StatusRecruiting
PhaseN/A
SponsorLungpacer Medical Inc.
Enrollment30
Study TypeINTERVENTIONAL
ConditionsARDS (Moderate or Severe); AHRF; Mechanically Ventilated ICU Patients
Interventions

Multi-center, randomized, controlled, open-label Phase 2 feasibility trial. Subjects on mechanical ventilation (MV) for acute hypoxemic respiratory failure (AHRF) with lung injury (including subjects who meet criteria for acute respiratory distress syndrome (ARDS)) will be randomized 2:1 to diaphragm neurostimulation-assisted ventilation (DNAV) using the AeroNova System plus lung-protective ven…

NCT06441760 — Simulation Trial of Telemedical Support for Paramedics

StatusRecruiting
PhaseN/A
SponsorBoston Medical Center
Enrollment420
Study TypeINTERVENTIONAL
ConditionsEmergencies; Cardiopulmonary Arrest; Acute Respiratory Failure; Status Epilepticus
Interventions;

In the United States, the current standard of prehospital (i.e. outside of hospitals) emergency care for children with life-threatening illnesses in the community includes remote physician support for paramedics providing life-saving therapy while transporting the child to the hospital. Most prehospital emergency medical services (EMS) agencies use radio-based (audio only) communication between…

NCT07685106 — Evaluation of the Effectiveness of the Cardiostory Device in Distinguishing Heart Failure From Other Causes in Patients Presenting With Dyspnea.

StatusRecruiting
PhaseN/A
SponsorCardioStory INC
Enrollment850
Study TypeOBSERVATIONAL
ConditionsHeart Failure; Dyspnea
Interventions

This is a prospective, observational study conducted in the emergency department. Adult patients presenting with dyspnea will be enrolled, and study data will be collected from routine clinical assessments, including medical history, physical examination, laboratory tests, and echocardiography results, as well as non-invasive cardiovascular measurements obtained using the CardioStory device.

NCT07307066 — Real-Time Algorithm-Driven Ventilation Feedback to Improve Lung-Protective Ventilation in Patients With ARDS (REALVENT-study)

StatusRecruiting
PhaseN/A
SponsorPeking Union Medical College Hospital
Enrollment208
Study TypeINTERVENTIONAL
ConditionsARDS (Acute Respiratory Distress Syndrome); VILI (Ventilator-induced Lung Injury); Respiratory Failure; Critical Illness
Interventions;

The REALVENT trial is designed to evaluate whether a real-time, algorithm-driven ventilation feedback strategy can improve lung-protective ventilation (LPV) achievement rates in critically ill patients receiving invasive mechanical ventilation. This multicentre randomised controlled trial will compare real-time respiratory waveform monitoring with automated feedback against standard ICU care. T…

NCT07379775 — Evaluation of the Reliability of AAR as an Independent Tool for Surgical Indication in Nasal Obstruction

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment200
Study TypeOBSERVATIONAL
ConditionsNasal Obstruction
Interventions

Nasal obstruction (NO) affects ~30% of the population and is a very common reason for consultation in otorhinolaryngology (ORL). In the majority of cases, the origin is inflammatory (allergic rhinitis and chronic rhinosinusitis) while in a minority of cases, the origin is structural, including septal deviation and inferior turbinate hypertrophy.

NO significantly impairs patients’ quality of l…

NCT06189924 — Exhaled Breath Condensate Analysis in Mechanically Ventilated Patients

StatusRecruiting
PhaseN/A
SponsorThe Institute of Molecular and Translational Medicine, Czech Republic
Enrollment200
Study TypeOBSERVATIONAL
ConditionsAcute Respiratory Failure; Critical Illness
Interventions

Mechanically ventilated intensive care patients will be sampled for a small amount of exhaled breath condensate from the ventilator circuit and for venous blood.

Proteomic analysis of the exhaled breath condensate will be performed using mass spectrometry and in the blood sample, corresponding changes in the DNA, RNA, proteins, and metabolites will be studied. Resulting profiles will be correl…

NCT07664930 — Phrenic Nerve and Diaphragm Electrophysiology in Pompe Disease

StatusRecruiting
PhaseN/A
SponsorIRCCS National Neurological Institute “C. Mondino” Foundation
Enrollment20
Study TypeOBSERVATIONAL
ConditionsPompe Disease

Pompe disease is traditionally considered a lysosomal myopathy. However, increasing experimental and clinical evidence suggests involvement of the entire motor unit, including motor neurons, peripheral nerves, neuromuscular junctions, and skeletal muscle. Respiratory impairment is a major cause of morbidity and mortality, and diaphragm dysfunction is frequently observed.

Clinical observations …

NCT07451977 — Effects of Oxygen Supplementation During the 6-Minute Walk Test in Chronic Respiratory Failure or Exertional Hypoxemia

StatusRecruiting
PhaseN/A
SponsorIstituti Clinici Scientifici Maugeri SpA
Enrollment114
Study TypeINTERVENTIONAL
ConditionsChronic Respiratory Failure; Hypoxemia; Chronic Obstructive Pulmonary Disease (COPD); Interstitial Lung Disease
Interventions;

The aim of this multicenter crossover trial is to describe the effect of adding a therapeutic dose of exertional oxygen therapy, in terms of exercise performance, gas exchange, heart rate, symptoms perception and subjective easiness of performance, in a cohort of subjects hospitalized in specialized pulmonary rehabilitation centers with a diagnosis of chronic respiratory failure and/or exertion…

NCT06819644 — Optimisation of High Flow Oxygen Therapy Settings During Hypoxaemic Respiratory Distress Based on Non-contact Measurement of Lung Volumes by Depth Camera

StatusRecruiting
PhasePhase 3
SponsorUniversity Hospital, Brest
Enrollment406
Study TypeINTERVENTIONAL
ConditionsHypoxemic Respiratory Failure
Interventions

The goal of this clinical trial is to validate the interest of a strategy adjusting the flow rate delivered under high-flow oxygen (HFO) therapy according to the lung volumes measured by a new technique, in intensive care patients with hypoxemic respiratory distress (HRD).

The main question it aims to answer is:

“The use of a technique of measurement of lung pulmonary with adjustement to the …

NCT07672106 — Assessment of Reintubation Risk Using Multiple Parameters in Postoperative Intensive Care Unit Patients

StatusRecruiting
PhaseN/A
SponsorProf. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Enrollment600
Study TypeOBSERVATIONAL
ConditionsPostoperative Respiratory Failure; Extubation Failure; Lung Ultrasonography Score; Diaphragm Thickness; Parasternal Intercostal Muscle Thickness

This prospective, non-interventional observational study will evaluate the risk of reintubation in adult postoperative patients admitted to the intensive care unit after major surgery. Reintubation after extubation is an important clinical problem because it may increase complications, prolong mechanical ventilation, and extend intensive care and hospital stay.

The study will include adult pat…

NCT07615010 — A Clinical Trial to Evaluate agenT-797 Plus Standard of Care in Participants With Severe Pneumonia With Moderate to Severe Acute Hypoxemic Respiratory Failure

StatusRecruiting
PhasePhase 2
SponsorMiNK Therapeutics
Enrollment90
Study TypeINTERVENTIONAL
ConditionsPneumonia
Interventions; ;

This clinical trial will evaluate the efficacy and safety of a single intravenous dose of agenT-797 administered in addition to standard of care (SOC), compared with placebo plus SOC, in reducing short-term mortality in adult participants with severe pneumonia and moderate to severe AHRF. All participants will receive SOC management for severe pneumonia and acute respiratory distress syndrome (…

NCT07071935 — A Clinical Trial of Early Ventilation in Amyotrophic Lateral Sclerosis (EVENT ALS)

StatusRecruiting
PhasePhase 2
SponsorUniversity of Pennsylvania
Enrollment48
Study TypeINTERVENTIONAL
ConditionsAmyotrophic Lateral Sclerosis (ALS); Chronic Respiratory Failure; Neuromuscular Disease Patients; Neuromuscular Disease; Respiratory Insufficiency
Interventions

Amyotrophic lateral sclerosis (ALS) is a disease that causes weakness of the muscles of the body. The disease can eventually lead to severe breathing problems, which is the most common cause of death from ALS. The treatment for breathing is non-invasive ventilation (NIV). It is a machine that helps a person breathe by pushing air in and out of their lungs through a mask worn over the face. Rese…

NCT07686315 — Advanced Respiratory Monitoring for Safer Mechanical Ventilation in Patients Without Respiratory Failure

StatusRecruiting
PhaseN/A
SponsorIstituto Clinico Humanitas
Enrollment40
Study TypeOBSERVATIONAL
ConditionsDeveloping Acute Respiratory Distress Syndrome
Interventions

Patients admitted to the intensive care unit (ICU) and mechanically ventilated for reasons other than acute respiratory failure, such as coma, trauma, or sepsis, are at risk of developing acute respiratory distress syndrome (ARDS), which increases the duration of mechanical ventilation, mortality, and functional dependence at discharge.

NCT07556185 — MedlyPeds Feasibility Study

StatusRecruiting
PhaseN/A
SponsorThe Hospital for Sick Children
Enrollment30
Study TypeINTERVENTIONAL
ConditionsPediatric Heart Failure; Congenital Heart Disease (CHD); Acquired Heart Disease; Pulmonary Hypertension; Post Cardiac Surgery
Interventions

SickKids and UHN have developed MedlyPeds which is a smart phone application designed to remotely monitor patients with heart disease. This is a feasibility study which will enroll up to 30 patients with different types of heart disease to see which patient types may benefit the most from MedlyPeds if it were to be used for clinical monitoring. The study is gathering feedback about the app from…

NCT07214376 — A Randomized Placebo-procedure Controlled Trial of the Enhancor System (PULmonary Artery Denervation) to Evaluate Safety and Efficacy in Patients With Combined Pre- and Post-capillary Pulmonary Hypertension Associated With Left Heart Disease

StatusRecruiting
PhaseN/A
SponsorPulnovo Medical, Inc.
Enrollment750
Study TypeINTERVENTIONAL
ConditionsPulmonary Hypertension; Heart Failure With Reduced Ejection Fraction; Hypertension; Vascular Diseases; Cardiovascular Diseases
Interventions;

The goal of this clinical study is to evaluate the safety and efficacy of percutaneous pulmonary artery denervation with the Multi-Pole Pulmonary Artery Radiofrequency Ablation Enhancor System in patients with combined pre- and post-capillary pulmonary hypertension (CpcPH) associated with left heart disease (LHD). This randomized control trial will compare the investigational device (The Enhanc…

Active, Not Recruiting

NCT02962557 — Detecting Post-surgical Respiratory Compromise and Prompting Patients to Self-rescue: An Early Feasibility Study

StatusActive, not recruiting
PhaseN/A
SponsorUniversity of Utah
Enrollment40
Study TypeINTERVENTIONAL
ConditionsAnesthesia
Interventions

This study will explore the feasibility of an idea to use standard, FDA-approved patient monitors to detect ventilatory depression and then play a recorded nurse’s voice to prompt patients by name to breathe. The voice prompt will occur in addition to when the traditional alarms are sounded by the monitors. The study device consists of commercially available physiologic monitors, a speaker, and…

NCT04212962 — Transitional Care Model Evaluation 2020

StatusActive, not recruiting
PhaseN/A
SponsorMathematica Policy Research, Inc.
Enrollment962
Study TypeINTERVENTIONAL
ConditionsCHF - Congestive Heart Failure; COPD; Pneumonia
Interventions;

The study is a randomized controlled trial to estimate the effects of the transitional care model (TCM) on hospital admissions and patients’ experience during the year following the patient’s qualifying discharge. The University of Pennsylvania, where TCM was developed, will be the coordinating center for the implementation. The study will be conducted in three large health systems spread throu…

NCT06616974 — A Study of TX000045 in Patients With Pulmonary Hypertension Secondary to Heart Failure With Preserved Ejection Fraction (the APEX Study)

StatusActive, not recruiting
PhasePhase 2
SponsorTectonic Therapeutic
Enrollment191
Study TypeINTERVENTIONAL
ConditionsPulmonary Hypertension; Heart Failure With Preserved Ejection Fraction
Interventions; ;

TX000045-003 is a double-blind, randomized, parallel group, placebo-controlled, proof- of-concept (POC) study, evaluating 2 dose regimens of TX000045 over the course of a 24-week treatment period (the APEX study).

Not Yet Recruiting

NCT07672041 — Inspiratory Muscle Training for People With Heart Failure

StatusNot yet recruiting
PhaseN/A
SponsorUniversidad Nacional Andres Bello
Enrollment108
Study TypeINTERVENTIONAL
ConditionsHeart Failure
Interventions; ;

Heart failure is frequently associated with inspiratory muscle weakness, which contributes to dyspnea, reduced exercise capacity, impaired quality of life, and adverse cardiovascular outcomes. Although inspiratory muscle training (IMT) is a recommended adjunct to cardiovascular rehabilitation, the optimal training modality remains uncertain, particularly among patients with reduced and preserve…

NCT07667829 — Vasopressor Agents in Pulmonary Hypertension Crisis

StatusNot yet recruiting
PhaseN/A
SponsorChina National Center for Cardiovascular Diseases
Enrollment75
Study TypeINTERVENTIONAL
ConditionsPulmonary Arterial Hypertension (PAH); Chronic Thromboembolic Pulmonary Hypertension (CTEPH); Hypertension, Pulmonary
Interventions; ;

Comparison of the efficacy and safety of three vasoactive agents-dopamine, norepinephrine, and epinephrine-in the treatment of patients with pulmonary hypertension crisis: prospective, randomised controlled trial monitored by haemodynamic monitoring

NCT07613918 — Brain Blood Flow and Cerebral Autoregulation Monitoring in Critically Ill Children

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Wisconsin, Madison
Enrollment125
Study TypeOBSERVATIONAL
ConditionsCritical Illness; Pediatric Critical Illness; Respiratory Failure; Traumatic Brain Injury; Cardiac Arrest
Interventions

This study uses a non-invasive (external) ultrasound test called Transcranial Doppler (TCD) to measure how blood flows through the major arteries of the brain of children receiving care in the Pediatric Intensive Care Unit (PICU). TCD is already used for clinical reasons in many children, but it is not part of routine monitoring for every critically ill child. By using TCD, the investigators ho…

NCT07679646 — Effectiveness and Efficiency of Home Telemonitoring and Non-invasive Ventilation in Patients With COPD and Hypercapnia (EVALECO)

StatusNot yet recruiting
PhaseN/A
SponsorAir Liquide Healthcare Spain
Enrollment92
Study TypeOBSERVATIONAL
ConditionsPulmonary Disease, Chronic Obstructive (COPD); Hypercapnia
Interventions

The purpose of this study is to evaluate the effectiveness and clinical efficiency of combining home non-invasive ventilation (NIV) with a continuous remote telemonitoring (TM) system in patients with Chronic Obstructive Pulmonary Disease (COPD) and persistent hypercapnia. In standard practice, patients with severe COPD and high carbon dioxide levels in their blood are treated with home non-inv…

NCT07679932 — Optimization of Respiratory Effort With Titrated Sedation in AHRF

StatusNot yet recruiting
PhaseN/A
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS
Enrollment40
Study TypeOBSERVATIONAL
ConditionsAHRF

Prospective, observational, monocentric study to assess the physiological effects of dexmedetomidine and remifentanil in spontaneously breathing patients with acute hypoxemic respiratory failure receiving high-flow nasal oxygen.

NCT07676786 — Euvolemia-Based Assessment of Pulmonary Hypertension in Stable Hemodialysis Patients

StatusNot yet recruiting
PhaseN/A
SponsorStefan Lujinschi
Enrollment30
Study TypeOBSERVATIONAL
ConditionsPulmonary Hypertension (PH); End Stage Kidney Disease (ESRD); Hemodialysis Patients; Volume Overload; Volume Assessment
Interventions

Pulmonary hypertension (PH) is a frequent and clinically significant complication in patients with end-stage kidney disease (ESKD) undergoing maintenance hemodialysis (HD). However, PH assessment in this population is often confounded by volume overload, leading to potential overestimation and misclassification.

This prospective, multicenter observational study aims to evaluate the prevalence,…

NCT07005297 — Clinical Genetics Branch Eligibility Screening Survey

StatusNot yet recruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1000
Study TypeOBSERVATIONAL
ConditionsMelanoma; Li-Fraumeni Syndrome; Pulmonary Blastoma; Chordoma; Congenital Bone Marrow Failure Syndromes

Background:

Clinical Genetics Branch (CGB) researchers study individuals and populations at high genetic risk of cancer in order to improve our understanding of cancer and to improve cancer care. There are currently 6 open clinical genetics studies at the CGB eligible for this screening process.

  • 02C0052: Etiologic Investigation of Cancer Susceptibility in Inherited Bone Marrow Failure Syndr…

NCT07603037 — EIT Evaluation of Different Antihypertensive Agents on the Ventilation-Perfusion Ratio in Patients With Acute Respiratory Failure

StatusNot yet recruiting
PhaseN/A
SponsorFirst Affiliated Hospital of Wannan Medical College
Enrollment12
Study TypeINTERVENTIONAL
ConditionsAcute Respiratory Failure (ARF); Hypertension; Pulmonary Perfusion Imbalance; Aortic Dissection (Subset)
Interventions;

This prospective, single-center interventional study aims to evaluate the effect of two commonly used intravenous antihypertensive agents - nicardipine and nitroglycerin - on lung ventilation-perfusion (V/Q) distribution in patients with acute respiratory failure complicated by hypertension. Electrical Impedance Tomography (EIT) will be used for noninvasive monitoring of pulmonary ventilation a…

NCT07634783 — Delta Pocc During Spontaneous Breathing Trial to Predict Extubation Failure in Mechanically Ventilated Adults (DELTA-EXT)

StatusNot yet recruiting
PhaseN/A
SponsorSanatorio Parque, Argentina
Enrollment120
Study TypeOBSERVATIONAL
ConditionsMechanical Ventilation Weaning From Mechanical Ventilation Extubation Failure Critical Illness
Interventions

This prospective observational single-center study will evaluate whether dynamic respiratory stress estimated by delta airway occlusion pressure deflection (Delta Pocc) during a standardized spontaneous breathing trial can predict extubation failure in mechanically ventilated adult intensive care unit patients.

Liberation from invasive mechanical ventilation is a critical step in ICU care. Alt…

NCT07675434 — Prospective Cohort of Acute Cardiology Referrals in an Ambulatory Day-Hospital Setting

StatusNot yet recruiting
PhaseN/A
SponsorAssistance Publique - Hôpitaux de Paris
Enrollment25000
Study TypeOBSERVATIONAL
ConditionsAcute Coronary Syndromes; Heart Failure; Pulmonary Embolism, Deep Vein Thrombosis; HTN-Hypertension; Arrhythmia

Suspected acute or subacute cardiovascular diseases-including chest pain, dyspnea, and palpitations-are among the most common reasons for unscheduled emergency department visits and pre-hospital referrals. Despite this high clinical burden, the diagnostic yield is often limited, with a frequent mismatch between initial clinical suspicion and final diagnosis, contributing to substantial healthca…

NCT07663799 — Wearable Assessment of Thoracic, Cardiac Health and Exercise Performance Trial Prospective

StatusNot yet recruiting
PhaseN/A
SponsorThe University of Hong Kong
Enrollment20
Study TypeOBSERVATIONAL
ConditionsCongenital Heart Disease; Pulmonary Hypertension; Heart Failure; Coronary Heart Disease (CHD); Apple Watch
Interventions

Wearable health technology, particularly smartwatches, has revolutionized personal health monitoring by enabling continuous, non-invasive tracking of various physiological parameters. The potential applications of these devices in cardiology are extensive, but it is crucial to validate their accuracy against established medical-grade devices.

The Apple Watch Series 9 (Apple, USA) exemplifies t…

NCT07673250 — Personalized Ventilator Settings for Patients on ECMO

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of California, San Diego
Enrollment62
Study TypeINTERVENTIONAL
ConditionsAcute Respiratory Distress Syndrome (ARDS); Extracorporeal Membrane Oxygenation; Respiratory Failure Patients Treated With ECMO; Respiratory Failure, ICU; Ventilator Induced Lung Injury
Interventions

While mechanical ventilation can be used to sustain life in those with lung injury, it, can further worsen lung injury or prevent lung healing resulting in high morbidity and mortality as seen in Acute Respiratory Distress Syndrome (ARDS).

Using extracorporeal membrane oxygenation (ECMO), the highest level of life support also known as the heart-lung machine, investigators may minimize injury …

NCT07634419 — Self-directed Mobile Mindfulness to Address ICU Survivors’ Psychological Distress

StatusNot yet recruiting
PhaseN/A
SponsorDuke University
Enrollment450
Study TypeINTERVENTIONAL
ConditionsCritical Illness; Heart Failure; Sepsis; Ards; Pneumonia
Interventions;

Serious acute heart and lung illnesses like heart failure, severe COVID, and sepsis often leave survivors struggling not only physically, but also with lasting depression, anxiety, and stress. These problems that are hard to treat because access to mental health care is often limited. To help address this, the researchers created Lift, a fully automated mindfulness program designed with patient…

Completed Trials

NCT03108118 — Diaphragm Injury and Dysfunction During Mechanical Ventilation

StatusCompleted
PhaseN/A
SponsorUniversity Health Network, Toronto
Enrollment50
Study TypeOBSERVATIONAL
ConditionsRespiratory Insufficiency; Diaphragm Injury; Mechanical Ventilation Complication

This study is designed to evaluate the relationship between diaphragm activity during mechanical ventilation and the development of ventilator-induced diaphragm dysfunction (VIDD). Diaphragm structure, activity, and function are monitored longitudinally over the first 7 days of mechanical ventilation.

StatusCompleted
PhasePhase 2
SponsorNational Heart, Lung, and Blood Institute (NHLBI)
Enrollment18
Study TypeINTERVENTIONAL
ConditionsTelomere Disease
Interventions

Background:

DNA is a structure in the body. It contains data about how the body develops and works. Telomeres are found on the end of chromosomes in DNA. Some people with short telomeres or other gene changes can develop diseases of the bone marrow, lung, and liver. Researchers want to see if low doses of the hormone drug danazol can help.

Objective:

To study the safety and effect of low dos…

NCT03629340 — Metformin for Pulmonary Hypertension HFpEF

StatusCompleted
PhasePhase 2
SponsorUniversity of California, San Francisco
Enrollment33
Study TypeINTERVENTIONAL
ConditionsPulmonary Hypertension; Heart Failure
Interventions;

The main objective of this study is to determine the clinical efficacy of metformin versus placebo and the therapeutic response with regards to functional capacity and hemodynamics in PH-HFpEF.

NCT04886128 — Improving Diagnostic Accuracy for Acute Heart Failure

StatusCompleted
PhaseN/A
SponsorVanderbilt University Medical Center
Enrollment2469
Study TypeOBSERVATIONAL
ConditionsAcute Heart Failure; Dyspnea; Dyspnea; Cardiac

Acute heart failure is a common reason for emergency department visits and hospitalization, but the diagnosis can be challenging because of non-specific symptoms and signs. The current diagnostic approach to acute heart failure has modest accuracy, leading to delayed diagnosis and treatment, which associate with worse prognosis. Prior work suggests diagnostic accuracy can be improved with the a…

NCT05352490 — Diagnosis of Heart Failure in Chronic Obstructive Pulmonary Disease Using the Lung Ultrasound

StatusCompleted
PhaseN/A
SponsorUniversity of Monastir
Enrollment350
Study TypeOBSERVATIONAL
ConditionsDyspnea; Decompensated Heart Failure ; COPD Exacerbation
Interventions

Acute Heart failure (AHF) is a common cause of acute exacerbation of chronic obstructive pulmonary disease (AECOPD). This association is frequently underestimated with regard to the difficulty of clinical diagnosis. The investigators expect that the application of the lung ultrasound could be useful in this issue.

NCT07660757 — Epidemiological Cluster Evaluation in Patients Admitted to Internal Medicine, With at Least One of the Following Diagnoses: Heart Failure, COPD, Renal Failure. The FADOI IN-CluDiMI Study

StatusCompleted
PhaseN/A
SponsorFadoi Foundation, Italy
Enrollment4500
Study TypeOBSERVATIONAL
ConditionsHeart Failure; Chronic Obstructive Pulmonary Disease (COPD); Chronic Kidney Disease (CKD)

Improved medical care has led to an increase in both the age and clinical complexity of patients admitted to Internal Medicine wards, characterized by multiple chronic diseases. Multimorbidity is a common issue in the elderly, significantly associated with higher mortality, functional decline, and poorer quality of life. The concept of “disease clustering” goes beyond simple multimorbidity or c…

NCT06304493 — REMINDers for Incentive Spirometry in PACU (REMIND-IS in PACU)

StatusCompleted
PhaseN/A
SponsorUniversity of Colorado, Denver
Enrollment231
Study TypeINTERVENTIONAL
ConditionsPostoperative Atelectasis; Postoperative Hypoxemia; Postoperative Pneumonia; Postoperative Pulmonary Complications; Patient Adherence
Interventions

The purpose of this study is to determine if the frequency of use of incentive spirometry during the stay in the Post-Anesthesia Care Unit (PACU) increases with visual and auditory electronic reminders, as compared to not having those reminders.

NCT06336252 — Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients

StatusCompleted
PhaseN/A
SponsorBispebjerg Hospital
Enrollment130
Study TypeINTERVENTIONAL
ConditionsCOPD; Heart Failure; Parkinson Disease; Arthritis; Old Age; Cachexia
Interventions

Primary Objective To investigate if patients hospitalised for older adults with a decreased level of physical function, either related to a chronic condition e.g., COPD, Congestive heart failure, renal failure; infections; frailty and tendency of falling; orthopaedic surgery - after hip fracture will increase their time spent out of bed during hospitalisation and 3 months after discharge throug…

NCT06114992 — Servo-n HFOV Study: Safety and Performance in Neonates and Infants

StatusCompleted
PhaseN/A
SponsorMaquet Critical Care AB
Enrollment83
Study TypeOBSERVATIONAL
ConditionsElective HFOV for Respiratory Failure in Neonates/Infants; Rescue HFOV in Neonates and/Infants With Refractory Respiratory Failure Under Conventional Therapy
Interventions

The purpose of this study is to evaluate the safety and performance of High-Frequency Oscillatory Ventilation (HFOV) modes of the Servo-n ventilator in neonates and infants, by using a prospective, observational, single-arm (i.e., non-controlled) and multi-center Post-Market Follow-up (PMCF) study design. HFOV treatment will be evaluated by assessing ventilation and oxygenation variables, and s…

NCT06574659 — Noninvasive Ventilation Breathing Test Guiding Weaning in Patients With Acute Hypoxic Respiratory Failure

StatusCompleted
PhaseN/A
SponsorWest China Hospital
Enrollment160
Study TypeINTERVENTIONAL
ConditionsAcute Hypoxic Respiratory Failure
Interventions;

SBT, as a routine extubation strategy for invasive mechanical ventilation, has been widely recognized. However, in recent years, studies have found that SBT may lead to delayed extubation, which has been confirmed in COPD patients but has not yet been widely accepted in patients with acute hypoxic respiratory failure. Both invasive mechanical ventilation and non-invasive mechanical ventilation …

NCT06960239 — Safety and Efficacy of the Irreversible Electroporation (IRE) System for Adenotonsillar Hypertrophy in Children

StatusCompleted
PhaseN/A
SponsorENTire Medical Ltd.
Enrollment31
Study TypeINTERVENTIONAL
ConditionsTonsillar Hypertrophy; Upper Airway Obstruction
Interventions

This is a multi-center, prospective, open-label, traditional feasibility study with a before-after study design. The study is designed to evaluate the safety and efficacy of an Irreversible Electroporation (IRE) System for the treatment of upper airway obstruction due to adenotonsillar hypertrophy in Children.

NCT06815523 — Prediction of Duration of Mechanical Ventilation in Acute Hypoxemic Respiratoty Failure

StatusCompleted
PhaseN/A
SponsorJesus Villar
Enrollment1241
Study TypeOBSERVATIONAL
ConditionsAcute Hypoxemic Respiratory Failure
Interventions

Acute hypoxemic respiratory failure (AHRF) is a common cause of admission in intensive care units (ICUs) worldwide. We will assess machine learning (ML) techniques for prediction of prolonged duration (> or = to 7 days) of mechanical ventilation (MV) in 1,241 patients enrolled in the PANDORA study in Spain. The study was registered with ClinalTrials.gov (NCT03145974). Our aim is to identify a …

NCT07411976 — Critical Care Admission Following Emergency Department’s Resuscitation Room Care

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Universitaire de Nīmes
Enrollment1629
Study TypeOBSERVATIONAL
ConditionsCritical Illness; Emergency Department Patient; Shock; Trauma (Including Fractures); Respiratory Failure
Interventions

This prospective multicenter observational study aims to describe resuscitation room activity in France and to compare critical care admission within 24 hours between patients directly admitted to the resuscitation room and those admitted secondarily after initial emergency department management. Adult patients admitted to the resuscitation room over a 72-hour period in participating centers wi…

Other (Terminated)

NCT02829736 — ThOracoscopic Wedge Resection Treated With Chest Tube Removal Intraoperatively

StatusTerminated
PhaseN/A
SponsorRigshospitalet, Denmark
Enrollment25
Study TypeINTERVENTIONAL
ConditionsPain; Decreased Lung Function; Delayed Discharge
Interventions; ;

Chest tubes are used routinely although preliminary studies demonstrate the feasibility and safety of intraoperative chest drain removal. Previous studies are however either retrospective or mainly concerning benign disease.

Hypothesis: Participants treated without post-operative chest tube after thoracoscopic wedge resection have less pain, better pulmonary function and similar complication p…