Respiratory Disease

20

Review clinical trials related to Respiratory Disease. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Prospective Multicenter Screening for Thoracic Disease Via Radiography

This multicenter, prospective study aims to evaluate the real-world clinical utility of chest X-ray (CXR) for large-scale thoracic disease screening. Adult participants presenting for health examinations will undergo digital CXR screening, and any suspected abnormalities will be confirmed via a gold standard reference, such as a chest CT scan or clinical follow-up. The primary outcome measure is the detection rate (screening yield) of confirmed thoracic conditions. Secondary measures will assess diagnostic accuracy (sensitivity and specificity), false-positive rates, and multi-center reading consistency. By providing prospective, large-cohort evidence, this research seeks to validate the cost-effectiveness and feasibility of CXR in identifying early-stage lung, pleural, and cardiac abnormalities, ultimately guiding public health strategies and optimizing early medical intervention.

Participants needed: 300,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chinese Academy of SciencesUpdated: May 13, 2026Locations: 1Duration: 5 Years
Eligibility criteria

Age over 18. [+2]

Women who are pregnant, lactating, or planning to become pregnant during the stu... [+3]

Status: Recruiting

A New Portable Device for Non-invasive Ventilatory Support

Acute respiratory failure is a medical emergency rapidly leading to death, if not timely treated. Prompt Continuous Positive Airway Pressure (CPAP) improves patient outcomes. However, pre-hospital CPAP is currently limited to healthcare providers due to the absence of easy-to-use and immediate devices specifically designed for the non-medical population. The efficacy and usability of a new portable CPAP device will be assessed. This device is specifically designed for potential use in out-of-hospital scenarios involving acute respiratory failure. The evaluation will focus not only on the performance of the device but also on its easiness of use.

Participants needed: 50
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Università Vita-Salute San RaffaeleUpdated: May 6, 2026Locations: 3
Eligibility criteria

Age ≥65 years [+3]

Hospitalized adult patient [+9]

Status: Recruiting

Symptoms, Respiratory Dysfunction and Frailty Level in Allergic and Eosonophilic Asthmatics

The aim of this study is to determine the level of respiratory dysfunction, symptoms and frailty in patients with asthma according to different endophenotypes (allergic and eosonophilic asthma). In the light of the data obtained, it is thought that rehabilitation approaches that can be determined according to different endophenotypes in line with the evaluated parameters will guide health professionals working in this field. Hypotheses H0: There is no difference between allergic and eosonophilic asthmatics in terms of pulmonary function, respiratory dysfunction, symptoms, dyspnoea, fatigue, rhinitis, perception of breathlessness in activities of daily living, asthma control, level of frailty or quality of life. H1: There is a difference between individuals with allergic and eosonophilic asthma in terms of pulmonary function, respiratory dysfunction, symptoms, dyspnoea, fatigue, rhinitis, perception of breathlessness in activities of daily living, asthma control, level of frailty or quality of life.

Participants needed: 60
Trial details
Age: 35-75Biological sex: AllType: ObservationalSponsor: Hacettepe UniversityUpdated: Dec 29, 2025Locations: 1
Eligibility criteria

Age between 35-75 years, [+1]

Known cognitive impairment, [+2]

Status: Recruiting

Procedural Skills Transfer in Bronchoscopy

Brief summary The goal of this Feasibility study is to capture bronchoscopy data from patients (Group1) and bronchoscopists (Group 2) over a period of three years. The investigators wish to collect the pre-procedure CT scans and endoscopy videos of 300 patients. Up to 20 bronchoscopists will take part in the study Primary outcomes 1. To collect imaging data from patients undergoing routine bronchoscopy procedures 2. To collect movement data from clinicians performing the routine bronchoscopy procedures using a sensory Glove Secondary outcomes 1. Integrate the data gathered with procedure guidelines to develop a representation of procedure success using machine learning algorithms. 2. Develop an actionable knowledge base for bronchoscopy skill transfer to novice/untrained medical staff. 3. Investigate the feasibility of developing models of bronchoscopy procedures to develop training tools in the future There are no additional samples or time commitments from the participants in Group 1. The participants in Group 2 will be asked to answer a short questionnaire about their experience in performing bronchoscopies and will be asked to wear a sensory glove during the bronchoscopy procedure to capture their hand movements.

Participants needed: 320
Trial details
Age: 16+Biological sex: AllType: ObservationalSponsor: University of EdinburghUpdated: Sep 11, 2025Locations: 1
Eligibility criteria

over 16 years of age [+3]

Clinicians who do not give consent to participate in the study [+1]

Status: Recruiting

How OMT Benefits Newly Diagnosed Patients With Respiratory Illness When Given Alongside Other Standard Care.

This study is to see Osteopathic Manipulative Therapy, or OMT, can aid in treating patients being seen for respiratory illness and associated symptoms. The hypothesis is that the addition of OMT therapy, alongside other standard care (such as a medication), can help lessen patient symptoms sooner than just other treatment alone, and the duration of the condition will shorten as well.

Participants needed: 68
Trial details
Age: 65-100Biological sex: AllType: InterventionalSponsor: Geisinger ClinicUpdated: Jul 8, 2025Locations: 1
Eligibility criteria

Patients being seen for respiratory illness symptoms at Geisinger 65-Forward Buc... [+2]

Patients that have a healing fracture, including the spine, pelvis, shoulder, ri... [+2]

Status: Recruiting

Caffeine as an Adjuvant Therapy for Late Preterm Infants With Respiratory Distress

Use of caffeine citrate in late-preterm infants with respiratory distress is questionable. Oliphant and colleagues found in a recently published study that caffeine therapy use in late-preterm infants at a loading dose of 20 and 40 mg/kg and maintenance dose of 10 and 20 mg/kg/day reduces the incidence of intermittent hypoxia events by 61 and 67% respectively. The investigators hypothesized that caffeine will improve respiratory drive, prevent apnea, shorten the hospital stay and improve arousal state in late preterm infants. The investigators aim to study the effect of caffeine citrate on late preterm babies as regard duration of respiratory support, duration of hospital stay, respiratory morbidity, incidence and frequency of apnea.

Participants needed: 134
Trial details
Phase: Phase 2, Phase 3Age: 1-3Biological sex: AllType: InterventionalSponsor: Ministry of Health, Saudi ArabiaUpdated: Jun 27, 2025Locations: 2
Eligibility criteria

Newborn infants at gestational age 34 0/7 through 36 6/7 [+1]

Status: Recruiting

Prospective Observational Study to Characterize Patients Treated at Internal Medicine Clinics

Patients referred to internal medicine wards are becoming increasingly complex and fragile. Despite deep knowledge of their specific disorders, steps are required to improve overall management of their acute and chronic conditions. The main objective of the study is to identify demographic, clinical, laboratory and radiological markers of disease severity and activity in patients with diseases treated at general medicine wards (respiratory disease, immune-mediated disease, sepsis, metabolic disease, rare disease, frailty, pregnancy pathology) in order to improve their diagnosis, monitoring and treatment processes.

Participants needed: 50,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: IRCCS San RaffaeleUpdated: Jun 22, 2025Locations: 2
Eligibility criteria

Receving treatment at internal medicine departments (inpatient, outopatient, day... [+7]

refusal to participate [+1]

Status: Not yet recruiting

The Effect of Vitamin E Supplementation on Hospital Stay Duration in Non-cyanotic Heart Disease Children With Lower Respiratory Tract Infections

Congenital heart disease can lead to serious health issues, particularly an increased risk of infections, specifically respiratory infections. Lower respiratory tract infections are the fifth leading cause of death globally. Also considered a significant cause of morbidity and mortality among children with congenital heart disease. In Egypt, it is estimated that 10% of deaths in children under the age of 5 years are probably caused by lower respiratory tract infections and other acute respiratory infections. common non-cyanotic CHD like Ventricular septal defect predispose to bronchopneumonia. Hemodynamically significant congenital heart disease with pulmonary congestion increases the risk of lower respiratory tract infections and hospitalizations. This relies on several modifiable risk factors, including low socioeconomic status, poor diet, overcrowding, prematurity, male gender, and exposure to secondhand smoke. Micronutrients play a crucial role in strengthening the immune system. Many Studies have shown that when children are supplemented with various micronutrients, they experience fewer episodes of acute respiratory infections, and the duration and severity of these infections are reduced. Vitamin E is essential for immune system function and may lower disease risk by enhancing immune responses. It protects neurons and respiratory mucosa from oxidative damage and has been linked to a reduced incidence of asthma and inflammation, potentially safeguarding young children from atopy and wheezing. There are no available studies in our locality about the effect of vitamin E supplementation on the length of hospital stay for non-cyanotic cardiac patients with lower respiratory tract infections.

Participants needed: 260
Trial details
Phase: Phase 4Age: 2-5Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: Apr 15, 2025
Eligibility criteria

Pediatric patients are diagnosed with non-cyanotic heart disease associated with...

Pediatric patients that have other congenital anomalies other than CHD. [+3]

Status: Not yet recruiting

Development of the Drug and Alcohol Respiratory Health Test

The goal of this study is to develop a brief Drug and Alcohol Respiratory Health Test (DARHT) and offer it for routine use in clinical assessment and medical reviews

Participants needed: 260
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: King's College LondonUpdated: Apr 10, 2025Locations: 1
Eligibility criteria

>18 (no upper age limit) [+2]

Reported physical health condition that would mean spirometry contra-indicated -... [+2]

Status: Recruiting

Frequent Standardized Oral Care Using Human Milk in the Neonatal Intensive Care Unit

Premature infants are susceptible to complications related to infrequent and non-standardized oral care. Although the benefits of frequent standardized oral care are known to reduce oral dysbiosis (increased level of potentially pathogenic bacteria) and its associated complications in critically ill adults leading to established evidence-based guidelines, no such information exists for VLBW infants. The proposed study will prospectively follow 168 VLBW infants for 4 weeks following birth.

Participants needed: 218
Trial details
Age: 1-3Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Apr 1, 2025Locations: 1
Eligibility criteria

Mother ≥18 years of age [+4]

Status: Recruiting

Extremely Preterm Respiratory Outcome Cohort

This study examines the respiratory outcomes of preterm infants born at gestational ages less than 29 weeks, spanning from birth to 24 months corrected age. It delves into the intricacies of respiratory function impairment attributable to diverse factors, such as respiratory distress syndrome, bronchopulmonary dysplasia, postnatal corticosteroids, ventilatory support, as well as nutritional aspect during NICU stay. Furthermore, it scrutinizes the incidence of chronic respiratory diseases stemming from these conditions, assessing their long-term impact on respiratory prognosis post-discharge. In addition to respiratory aspects, the research extends its focus to the growth and developmental outcomes of preterm infants. By synthesizing these multifaceted elements, the study aspires to enhance current treatments and preventative measures for respiratory conditions in preterm infants.

Participants needed: 600
Trial details
Age: Up to 7Biological sex: AllType: ObservationalSponsor: Seoul National University HospitalUpdated: Dec 10, 2024Locations: 1Duration: 6 Years
Eligibility criteria

Infants born at gestational age less than 29 weeks with cohort consent obtained...

death within 3 days of birth [+4]

Status: Recruiting

REVIVe: Frailty, Rehabilitation, and Outcomes in Critically Ill Adult and Pediatric Survivors of COVID-19 or ARI

Background: Many adults and some children with COVID-19 or acute respiratory infection become critically ill and need advanced life support in the Intensive Care Unit (ICU). Frailty is a medical condition of reduced function and health. Adults with frailty have a lower chance of surviving critical illness. The investigators are still learning about critically ill adults with COVID-19 or acute respiratory infection, and do not have much information on how frailty affects outcomes in critically ill children, with or without COVID-19 or acute respiratory infection. Rehabilitation can help survivors of COVID-19 or acute respiratory infection by improving strength and improve quality of life (QOL). Objectives: The main goal of this research study is to see if patients with frailty have a lower chance of surviving COVID-19 or acute respiratory infection critical illness and more health problems after survival than patients without frailty. The investigators will also study the types of rehabilitation received by patients with COVID-19 or acute respiratory infection. Methods: The investigators will include adults and children with COVID-19 or acute respiratory infection who are admitted to the ICUs that participate in the study. The investigators will gather data about each patient, including before and during their illness. Outcomes: The investigators will collect level of frailty, function, and types of therapy, or rehabilitation received by patients. In adults, the investigators are most interested in learning if frailty influences mortality, or death. In children, the investigators are most interested in whether children with COVID-19 or acute respiratory infection critical illness are more likely to develop frailty. The investigators will also study post-hospital discharge location in survivors (e.g., home, rehabilitation). Relevance: The COVID-19 pandemic is a global public health crisis. It is critical to understand how COVID-19 and other acute respiratory infection critical illness affects groups of people who are at higher risk, and the impact on outcomes that are important to patients, like functioning and QOL. The results will help policy makers plan post-hospital services for survivors, help healthcare workers understand the importance of rehabilitation practice for patients with COVID-19 or acute respiratory infection, and help researchers develop treatments to improve QOL after COVID-19 or acute respiratory infection.

Participants needed: 900
Trial details
Biological sex: AllType: ObservationalSponsor: McMaster UniversityUpdated: Nov 6, 2024Locations: 28
Eligibility criteria

Adult and pediatric survivors of COVID-19 or acute respiratory infection admitte...

Patients who were admitted to ICU for <24 hours

Status: Recruiting

INSPIRE Respiratory Health Program in Botucatu, São Paulo, Brazil

The goal of this observational study is to evaluate the implementation of the INSPIRE program and to plan actions for the preparation, coordination, monitoring, diagnosis, and treatment of respiratory diseases in the municipality of Botucatu. Methods: Individuals with respiratory symptoms from the municipality of Botucatu, aged 18 or older, will be invited to participate in the study, and socioeconomic data, as well as information on sex, gender, race, nutritional risk, frailty, tobacco exposure, and its derivatives, will be collected. For those with exposure, screening and treatment for respiratory diseases will be offered through assessment of pulmonary function, body composition, respiratory and peripheral muscle strength. Additionally, individuals over 40 years old with tobacco exposure equal to or greater than 30 pack-years will be offered low-dose chest CT screening for lung cancer. Expected results: To identify and assess vulnerable groups that face difficulties in accessing respiratory healthcare, as well as implement specific strategies for the treatment of respiratory diseases and tobacco control for these groups. To ensure equitable access to respiratory health for the entire population at risk due to smoking. Moreover, through proactive and reactive risk reduction actions implemented by the program, to intervene in distinct groups and other regions.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: UPECLIN HC FM Botucatu UnespUpdated: Nov 4, 2024Locations: 1Duration: 5 Years
Eligibility criteria

Age equal to or greater than 18 years old; [+3]

Difficulty understanding the issues addressed [+2]

Status: Recruiting

Sleepiz One+ vs. Capnography and Electrocardiography

Respiratory Rate (RR) and heart rate (HR) are vital signs crucial for assessing a patient's overall health, providing insights into various conditions and stressors. Effective management of chronic diseases relies on detecting pathological changes early, with RR being among the most sensitive predictors of patient deterioration. Therefore, vigilant monitoring of RR and HR is vital for improving patient outcomes. The primary aim of this study is to provide a thorough comparison of the performance of Sleepiz One+ algorithms and end-tidal carbon dioxide measurement (EtCO2) Capnography for measuring respiration rate and electrocardiography (ECG) for measuring heart rate, in healthy adults and patients suffering from chronic conditions (e.g., hypertension, Chronic Obstructive Pulmonary Disease (COPD), asthma, diabetes), at rest in a clinical setting when the data is acquired with the new hardware version. Additionally, the investigators will evaluate the performance of RR estimation against the thoracic effort belt and the HR against the pulse oximetry.

Participants needed: 35
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Sleepiz AGUpdated: Aug 26, 2024Locations: 1
Eligibility criteria

Age >=18years [+5]

Previous enrolment into the current study, [+8]

Status: Recruiting

The Gut-Lung Axis and Respiratory Illness in Children

The goal of this single-centre observational study conducted at the Royal Hospital for Children in Glasgow, Scotland, is to employ a multi-omics approach to investigate the "gut-lung axis" in health and disease. Part A is a cross-sectional study design investigating the postulated bidirectional link between the gut and lung microbiomes in children suffering from respiratory or gastrointestinal conditions. Children with no GI or respiratory issues attending for orthopaedic care will be used as a benchmark for a healthy gut-lung axis. The main questions we aim to answer are: * What does a healthy gut-lung axis look like? * Do children with respiratory issues show an altered gut microbiome? * Do children with GI issues show an altered lung microbiome? Part B is a longitudinal study design, that aims to assess the effects of biologics on the gut-lung axis by comparing the gut and lung microbiomes in children with asthma at two time-points who are indicated to start biologics therapy (Asthma treatment) or will not receive biologics therapy (asthma control). Participants will provide: * airway samples (to investigate the lung microbiome) * blood samples (to assess inflammatory and metabolic factors which may mediate communication between the two sites) whilst under general anaesthetic for a treatment related to their standard of care * stool samples (to assess gut microbiome) * dietary information (food diary and/or food frequency questionnaire) to assess relationships between diet and the gut-lung axis.

Participants needed: 150
Trial details
Age: 0-16Biological sex: AllType: ObservationalSponsor: NHS Greater Glasgow and ClydeUpdated: Feb 21, 2024Locations: 1
Eligibility criteria

Any infant/child/young person admitted to the RHC, Glasgow for an elective bronc... [+4]

Use of antibiotics by the day of admission or have used antibiotics in the previ... [+4]

Status: Recruiting

A Clinical Study to Map the HLA Genomic Region in the Greek Population

The aim of GENESIS clinical study is to map the HLA genomic region in the Greek population and evaluate possible correlations with selected underlying diseases.

Participants needed: 12,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Athens LifeTech ParkUpdated: Jan 26, 2024Locations: 8
Eligibility criteria

possess a Greek social security number and are visiting hospitals/clinics, and/o... [+1]

Subjects not able to provide written informed consent (e.g. ICU patients, mental... [+5]

Status: Not yet recruiting

Isotonic Saline for Children With Bronchiolitis

The goal of this randomized clinical trial is to investigate the optimal supportive treatment of bronchiolitis in infants from 0-12 months of age. The main question\[s\] it aims to answer are: * To investigate whether isotonic saline should be used as supportive treatment for children with bronchiolitis, and if so, identify the optimal route of administration. The primary outcome is duration of hospitalization. * To investigate the current epidemiology of the viral pathogens causing bronchitis in children in Denmark, and to assess whether children infected with specific pathogens might benefit from treatment with isotonic saline. The children are randomized after inclusion through computer randomization to one of the 3 arms in the study: 1. Nebulized isotonic saline 2. Nasal irrigation with isotonic saline 3. No treatment with saline The investigators will compare treatment with saline (both methods) with no treatment, and the investigators will also compare the two methods of delivery of saline (nebulized vs. nasal irrigation).

Participants needed: 300
Trial details
Age: 1-12Biological sex: AllType: InterventionalSponsor: Slagelse HospitalUpdated: Jun 15, 2023
Eligibility criteria

Runny nose [+7]

Children with cystic fibrosis or other serious congenital lung diseases [+1]

Status: Recruiting

Measures of Respiratory Health Registry

There are many techniques that can allow for the quantification of lung function in children; some are being used clinically and others are under development. Many of these tools are available at BC Children's Hospital. This registry study will act as a central repository for the results of traditional and novel pulmonary function tests done at BC Children's Hospital to allow for future analysis.

Participants needed: 1,000
Trial details
Age: 0-99Biological sex: AllType: ObservationalSponsor: University of British ColumbiaUpdated: Aug 15, 2022Locations: 1
Eligibility criteria

Physical findings at the screening that would compromise the safety of the parti... [+11]

Status: Recruiting

Imaging Measures of Respiratory Health Registry

This is a prospective, observational cohort registry that aims to collect data on pulmonary structure and function in healthy people and those with respiratory disease, using structural and functional pulmonary 1H-MRI and hyperpolarized 129Xe-MRI. Outcome measures generated from MRI may include but are not limited to measures of regional ventilation, pulmonary microarchitecture, and regional gas exchange. Additionally, one of the goals of the registry is to facilitate the development of novel image analysis techniques that have not yet been invented. These data will be stored along with demographic data, clinical data, and pulmonary function testing (PFT) data. This is an open registry. Eligible local and international investigators/institutions can apply for access.

Participants needed: 1,000
Trial details
Age: 0-99Biological sex: AllType: ObservationalSponsor: University of British ColumbiaUpdated: Nov 2, 2021Locations: 2Duration: 10 Years
Eligibility criteria

Physician-diagnosed lung disease - based on a diagnosis made by a treating staff... [+3]

Physical findings at screening that, in the opinion of the Investigator, would c... [+12]

Status: Recruiting

Hamburg City Health Study - a German Cohort Study

The Hamburg City Health Study (HCHS) is a large, prospective, long-term, population-based cohort study and a unique research platform and network to obtain substantial knowledge about several risk and prognostic factors in major chronic diseases.

Participants needed: 45,000
Trial details
Age: 45-74Biological sex: AllType: ObservationalSponsor: Universitätsklinikum Hamburg-EppendorfUpdated: May 2, 2019Locations: 1
Eligibility criteria

Inhabitant of the city of Hamburg at the time of inclusion into the study (Inclu... [+2]

Insufficient knowledge of the German language, in order to understand study docu... [+1]