Pulmonary Edema

9

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

Condition / disease
Location
Status: Not yet recruiting

Evaluating the Use of Prehospital Lung Ultrasound in EMS: A Multicenter Pilot Study

The goal of this prospective nonrandomized study is to determine if prehospital lung ultrasound findings result in a change in patient management. This study will look at how lung ultrasound exam improves diagnosis of respiratory distress in patients being treated by Emergency Medical Services, such as patients with heart failure. Additional questions include: * How well can paramedics obtain and interpret ultrasound images? * How does ultrasound use change treatment received by patients? * How does ultrasound use impact patient outcomes? Participants will receive a lung ultrasound exam, but otherwise receive standard evaluation and care. Patients who receive ultrasound will be compared to those who did not receive ultrasound for logistical reasons and patients from before the use of ultrasound. Ultrasound will not be withheld from any patient for the purposes of the study.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Jul 13, 2026Locations: 2
Eligibility criteria

Patient treated by Emergency Medical Services [+6]

Pediatric patients (<18) [+3]

Status: Recruiting

Systolic Function and Weaning-induced Pulmonary Edema (SystoWean Study)

The purpose of this study is to determine if the left and right ventricular systolic function is involved in the development of weaning failure related to weaning-induced pulmonary edema.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire de NiceUpdated: May 22, 2026Locations: 3
Eligibility criteria

Invasive mechanical ventilation for more than 48 hours [+6]

Age <18 years and pregnant women [+6]

Status: Not yet recruiting

Evaluating the Feasibility of Prehospital Lung Ultrasound

The goal of this prospective nonrandomized study is to determine if a lung ultrasound exam improves diagnosis of respiratory distress in patients being treated by Emergency Medical Services. The main question it aims to answer is whether ultrasound use increases likelihood of correctly diagnosing heart failure. Additional questions include: * How well can paramedics obtain and interpret ultrasound images? * How does ultrasound use change treatment received by patients? * How does ultrasound use impact patient outcomes? Participants will receive a lung ultrasound exam, but otherwise receive standard evaluation and care. Patients who receive ultrasound will be compared to those who did not receive ultrasound for logistical reasons and patients from before the use of ultrasound. Ultrasound will not be withheld from any patient for the purposes of the study.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Rutgers, The State University of New JerseyUpdated: Apr 24, 2026Locations: 2
Eligibility criteria

Patient treated by Emergency Medical Services [+6]

Pediatric patients (<18) [+3]

Status: Recruiting

Optimized Treatment of Pulmonary Edema or Congestion

Background: Intravenous (IV) loop-diuretics have been a key component in treating pulmonary edema since the nineteen sixties and has a Class 1 recommendation in the 2021 European Society of Cardiology guidelines for heart failure. Conversely, vasodilation was downgraded in the treatment of acute heart failure due to a lack of trials that compare vasodilation with loop-diuretics in a hyperacute clinical setting. This clinical equipoise will be tested in a trial including patients with pulmonary congestion immediately at hospital admission. Primary objective: To determine the superior strategy of loop-diuretics (furosemide), vasodilation (nitrates) or the combination during emergency treatment. Design: Investigator-initiated, randomized, double-blinded, placebo-controlled trial with 1:1:1 allocation. Intervention: Intervention-phase will last 6 hours from study-inclusion, and patients will be allocated to one of three groups: * Boluses of 40 mg IV furosemide + nitrate-placebo as soon as possible and repeated up to 10 times. * Boluses of 3 mg IV isosorbide dinitrate + furosemide-placebo as soon as possible. * Boluses of both 3 mg IV isosorbide dinitrate + of 40 mg as soon as possible.

Participants needed: 1,104
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Rigshospitalet, DenmarkUpdated: Apr 22, 2026Locations: 4
Eligibility criteria

Age ≥ 18 years [+5]

More than 40 mg IV furosemide within the last three hours before randomization i... [+3]

Status: Recruiting

Clinical Utility of Portable Dynamic Chest X Ray (DDR) in the ICU

Dynamic digital radiography (DDR) is a new advanced version of chest radiography that captures dynamic images at a rate of 15 frames per second. It is coupled with an analytical software that allows it to provide more advanced measures of lung motion, ventilation, and perfusion compared to traditional chest radiography. While implementation of DDR fixed machines are beginning elsewhere in the US, this trial involves the first applications of an FDA-approved portable DDR machine, for use at the bedside in the ICU. The goal of this clinical trial is to determine the feasibility and safety of portable DDR technology in the ICU, as well as to evaluate the improved clinical diagnostic value of the portable DDR system over current standards of care. Participants will receive one to three sets of DDR images, which will then be compared to their clinical gold standard exams (such as chest x-rays, CTs, or VQ scans) to assess and improve the precision and accuracy of measurements such as diaphragmatic motion, lung movement, and perfusion.

Participants needed: 230
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Oct 29, 2025Locations: 1
Eligibility criteria

Adults (at least 18 years of age) including both intubated/ventilated and non-in... [+2]

Special populations, including women with known pregnancy, prisoners, or institu... [+3]

Status: Recruiting

Cardiac Function in Swimming-Induced Pulmonary Edema (SIPE)

Acute or chronic cardiac dysfunction could be a contributing factor to swimming-induced pulmonary edema (SIPE). Knowledge on cardiac function in SIPE is limited and recommendations for cardiac evaluation of patients with SIPE are lacking. The present study was designed to assess cardiac function in patients with SIPE and in asymptomatic swimmers.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Dalarna County Council, SwedenUpdated: Feb 27, 2025Locations: 1
Eligibility criteria

respiratory symptoms during or after swimming at the Vansbrosimningen open water... [+6]

declined consent [+1]

Status: Recruiting

PEP-device for Treatment of Swimming-induced Pulmonary Edema (SIPE)

In swimming induced pulmonary edema (SIPE), there is a lack of knowledge regarding optimal treatment. The present study was designed to assess the benefit of treatment with positive expiratory pressure device (PEP-device) compared to spontaneous recovery in patients with SIPE without hypoxia in the out-of-hospital environment.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Dalarna County Council, SwedenUpdated: Feb 27, 2025Locations: 1
Eligibility criteria

clinical diagnosis of swimming induced pulmonary edema (SIPE) with need of acute... [+3]

declined consent [+3]

Status: Recruiting

O2 Versus CPAP Treatment of Patients Undergoing SIPE Therapy (OCTOPUS)

In swimming induced pulmonary edema (SIPE), there is a lack of knowledge regarding optimal treatment. The present study was designed to assess the benefit of continuous positive airway pressure (CPAP) compared to oxygen as a first line treatment of SIPE in the out-of-hospital environment.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Dalarna County Council, SwedenUpdated: Feb 27, 2025Locations: 1
Eligibility criteria

clinical diagnosis of swimming induced pulmonary edema (SIPE) with need of acute... [+2]

declined consent [+3]

Status: Recruiting

Screening for Individual Susceptibility Factors to Immersion Pulmonary Edema

Immersion Pulmonary Edema (IPE) is a relatively new form of hemodynamic pulmonary edema. The number of cases has been increasing over the last ten years and it has become the second most common cause of hospitalization for military divers, after decompression sickness. The pathophysiological mechanisms of IPE are not completely known. Its occurrence is linked to a combination of factors related to the environmental constraints of diving, as well as to the diver's equipment. The main external factors are increased hydrostatic pressure, cold, intense effort and emotional stress. The impact of internal factors is not known. At this time, no severe forms of IPE have been identified in the military. However, it is important to identify this pathology at an early stage, even if the signs appear minor, because the continuation of underwater activity can significantly worsen the clinical picture. The risk of recurrence (greater than 15%) could result in a severe or even lethal accident.

Participants needed: 63
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Direction Centrale du Service de Santé des ArméesUpdated: Sep 14, 2022Locations: 2
Eligibility criteria

Military or civilian diver with at least 100 dives [+2]

Divers with a current temporary medical incapacity to dive [+2]