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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Pennsylvania |
| Enrollment | 478 |
| Study Type | INTERVENTIONAL |
| Conditions | Extubation 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
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Beth Israel Deaconess Medical Center |
| Enrollment | 1100 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Connecticut Children’s Medical Center |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Respiratory 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Medical Center Groningen |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Chronic 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)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | CSPC Megalith Biopharmaceutical Co.,Ltd. |
| Enrollment | 380 |
| Study Type | INTERVENTIONAL |
| Conditions | EGFR-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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Lungpacer Medical Inc. |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | ARDS (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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Boston Medical Center |
| Enrollment | 420 |
| Study Type | INTERVENTIONAL |
| Conditions | Emergencies; 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.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | CardioStory INC |
| Enrollment | 850 |
| Study Type | OBSERVATIONAL |
| Conditions | Heart 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)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Peking Union Medical College Hospital |
| Enrollment | 208 |
| Study Type | INTERVENTIONAL |
| Conditions | ARDS (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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Nasal 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Institute of Molecular and Translational Medicine, Czech Republic |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | IRCCS National Neurological Institute “C. Mondino” Foundation |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Pompe 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istituti Clinici Scientifici Maugeri SpA |
| Enrollment | 114 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic 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
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | University Hospital, Brest |
| Enrollment | 406 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypoxemic 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization |
| Enrollment | 600 |
| Study Type | OBSERVATIONAL |
| Conditions | Postoperative 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
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | MiNK Therapeutics |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Pneumonia |
| 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)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University of Pennsylvania |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Amyotrophic 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Istituto Clinico Humanitas |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | Developing 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Hospital for Sick Children |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Pediatric 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
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Pulnovo Medical, Inc. |
| Enrollment | 750 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Utah |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Anesthesia |
| 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
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Mathematica Policy Research, Inc. |
| Enrollment | 962 |
| Study Type | INTERVENTIONAL |
| Conditions | CHF - 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)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Tectonic Therapeutic |
| Enrollment | 191 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Universidad Nacional Andres Bello |
| Enrollment | 108 |
| Study Type | INTERVENTIONAL |
| Conditions | Heart 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | China National Center for Cardiovascular Diseases |
| Enrollment | 75 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Wisconsin, Madison |
| Enrollment | 125 |
| Study Type | OBSERVATIONAL |
| Conditions | Critical 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)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Air Liquide Healthcare Spain |
| Enrollment | 92 |
| Study Type | OBSERVATIONAL |
| Conditions | Pulmonary 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | AHRF |
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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Stefan Lujinschi |
| Enrollment | 30 |
| Study Type | OBSERVATIONAL |
| Conditions | Pulmonary 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Melanoma; 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | First Affiliated Hospital of Wannan Medical College |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute 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)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sanatorio Parque, Argentina |
| Enrollment | 120 |
| Study Type | OBSERVATIONAL |
| Conditions | Mechanical 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 25000 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | The University of Hong Kong |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Congenital 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of California, San Diego |
| Enrollment | 62 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute 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
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 450 |
| Study Type | INTERVENTIONAL |
| Conditions | Critical 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University Health Network, Toronto |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Respiratory 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.
NCT03312400 — Low-Dose Danazol for the Treatment of Telomere Related Diseases
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Telomere 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
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | University of California, San Francisco |
| Enrollment | 33 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Vanderbilt University Medical Center |
| Enrollment | 2469 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute 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
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Monastir |
| Enrollment | 350 |
| Study Type | OBSERVATIONAL |
| Conditions | Dyspnea; 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Fadoi Foundation, Italy |
| Enrollment | 4500 |
| Study Type | OBSERVATIONAL |
| Conditions | Heart 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)
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Colorado, Denver |
| Enrollment | 231 |
| Study Type | INTERVENTIONAL |
| Conditions | Postoperative 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Bispebjerg Hospital |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD; 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Maquet Critical Care AB |
| Enrollment | 83 |
| Study Type | OBSERVATIONAL |
| Conditions | Elective 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
| Status | Completed |
| Phase | N/A |
| Sponsor | West China Hospital |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Acute 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
| Status | Completed |
| Phase | N/A |
| Sponsor | ENTire Medical Ltd. |
| Enrollment | 31 |
| Study Type | INTERVENTIONAL |
| Conditions | Tonsillar 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Jesus Villar |
| Enrollment | 1241 |
| Study Type | OBSERVATIONAL |
| Conditions | Acute 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
| Status | Completed |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nīmes |
| Enrollment | 1629 |
| Study Type | OBSERVATIONAL |
| Conditions | Critical 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
| Status | Terminated |
| Phase | N/A |
| Sponsor | Rigshospitalet, Denmark |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain; 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…