COVID-19 Respiratory Infection

9

Review clinical trials related to COVID-19 Respiratory Infection. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Light-based Immunomodulation for Guarding Against Human Respiratory Tract Infections

The purpose of trial is to determine if daily usage of a photobiomodulation device will decrease the incidence of upper respiratory tract infections (URI) due to COVID, influenza or other viruses.The RD-X10 device is handheld, can be self-administered, and has been shown to be safe in invivo studies.

Participants needed: 130
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: David MossUpdated: May 28, 2026
Eligibility criteria

Active Duty and DoD Beneficiaries (i.e. former military, spouse, dependent child...

Unable to comfortably insert RD-X19 into the mouth and keep in place for 5 minut... [+2]

Status: Recruiting

Cardiac Magnetic Resonance Tissue Characterization in COVID-19 Survivors

The purpose of this study is to test if visualizing the heart with cardiac MRI/echo will be important in the understanding cardiac function and prediction of cardiopulmonary symptoms, physical effort tolerance, and outcomes in COVID-19 survivors. If successful, the research will allow us to identify the causes of lasting cardiopulmonary symptoms and begin developing cardiac and lung directed therapies accordingly.

Participants needed: 510
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Weill Medical College of Cornell UniversityUpdated: Jan 22, 2026Locations: 3
Eligibility criteria

Emergency room presentation and/or hospitalization with COVID-19 infection defin...

Contraindication to CMR (i.e. non-compatible pacemaker/defibrillator) or gadolin... [+4]

Status: Recruiting

Passive Detection- SARS-CoV-2 (COVID-19) A&M Breathalyzer (PROTECT Kiosk) for Operational Medicine

The primary objective of this effort will be to optimize and operationalize innovative passive surveillance systems and in parallel, the effort will identify, evaluate, and transition groundbreaking new technologies in diagnostics for operationalization. To meet the objective and execute the deliverables for this program of effort, the A\&M Breathalyzer PROTECT Kiosk will be tested, modified and validated at Brooke Army Medical Center (BAMC). The collaborative efforts between the PI, Dr. Michael Morris at BAMC and Co-Investigator Dr. Tony Yuan at USU- Center for Biotechnology (4D Bio3) will assess the passive detection technology and provide a capability survey of use-case scenarios for different operational settings. Goals: 1. Optimization and operationalize the A\&M Breathalyzer PROTECT Kiosk, portable mass spectrometer (MS) Detector for Deployment in Military Operational Medicine Environments. The Breathalyzer will be deployed to BAMC to test its detection capabilities of COVID-19 among symptomatic and asymptomatic COVID-19 carrier vs. those not infected compared to gold standard RT-PCR. 2. Evaluate the passive sensing, breath capture system, built within the A\&M Breathalyzer PROTECT Kiosk. The conversion of the active breath capture system, currently requires a straw that the subject breaths into, where then a series of sensors built in the Breathalyzer would automatically sample the exhaled breath within proximity for recent COVID-19 exposure. This task would conclude with a set of sensors and sensor inputs that would be analyzed by the Atomic AI platform built in the device. Field testing at BAMC is planned to determine the level of detection and discrimination for sensor combinations to SARS-CoV2 components and biomarkers detected. This testing would update the Atomic AI algorithm, within the device, to understand the accuracy of positive detection and the resulting sensitivities.

Participants needed: 100
Trial details
Age: 18-89Biological sex: AllType: ObservationalSponsor: The Geneva FoundationUpdated: Dec 10, 2025Locations: 1
Eligibility criteria

Asymptomatic and symptomatic individuals 18 years and older [+3]

Any individual under age of 18 [+2]

Status: Recruiting

Respiratory Virus Metagenomics After COVID-19

The study aims to characterize the distributive pattern of viruses in upper airway and its relationship with influenza seasons, symptomatology and exposure setting. A total of 500 adults residing in Hong Kong would be recruited, who would complete a questionnaire and return self-collected nasal and throat swabs for metagenomic analyses.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chinese University of Hong KongUpdated: Jan 24, 2025Locations: 1
Eligibility criteria

adults normally residing in Hong Kong [+2]

individuals with mental illness [+1]

Status: Recruiting

Multicenter Randomized Double-blind Placebo-controlled Study to Investigate Azvudine in Symptomatic Adults With COVID-19 at Increased Risk of Progressing to Severe Illness

To investigate whether treatment with Azvudine reduces the risk of severe illness or death in patients who are at a potential risk of progressing to severe COVID-19 infection.

Participants needed: 1,096
Trial details
Phase: Phase 2, Phase 3Age: 18-120Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Nov 25, 2024Locations: 1
Eligibility criteria

Age ≥ 60 years; [+6]

(1) Known or suspected allergy to the components of Azvudine Tablets; (2) Patien...

Status: Recruiting

Trial of Venovenous ECMO to De-Sedate, Extubate and Mobilise in Hypoxic Respiratory Failure

To determine whether a strategy of adding venovenous ECMO to mechanical ventilation, as compared to mechanical ventilation alone, increases the number of intensive care free days at day 60, in patients with moderate to severe acute hypoxic respiratory failure.

Participants needed: 140
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Australian and New Zealand Intensive Care Research CentreUpdated: Aug 9, 2024Locations: 7
Eligibility criteria

Patients ≥18 to 65 years old [+4]

The patient will be extubated today or tomorrow (i.e. will not remain intubated... [+13]

Status: Recruiting

Evolution of Respiratory Function in Lung Transplant Patients With Moderate to Severe Covid-19 Infection

The SARS-Cov-2 infection pandemic has caused a large number of acute respiratory failures and deaths across the world. Certain factors have been identified as associated with a higher risk of developing a severe form and dying. Immunosuppression has been identified as a risk factor for progressing to a severe form. Lung transplant patients were particularly vulnerable during this period, with a high frequency of respiratory compromise, sometimes progressing towards acute respiratory distress syndrome and, at a later stage, towards fibrotic forms. The impact of the infection on the immunological status of the patient and on the tolerance of the transplant have been little studied. The various treatments implemented during the pandemic have rapidly evolved (immunotherapy, vaccination, convalescent plasma transfusion, etc.) which may have modulated this risk. The evolution of respiratory function may be linked to the respiratory infection itself, or to the severity of respiratory damage during the infection. It is therefore relevant to compare patients with a moderate form of COVID-19 (non-intubated patients) to patients with severe forms, requiring invasive ventilation in intensive care. The evolution of respiratory function after infection has not yet been studied.

Participants needed: 75
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, Strasbourg, FranceUpdated: Jul 8, 2024Locations: 1
Eligibility criteria

Adult patient [+5]

Subject having expressed his opposition to the reuse of his data for scientific...

Status: Not yet recruiting

Efficacy and Safety Study of Essential Oil-Based Preparation Administered to COVID-19 Patients

The aim of this study was to compare the efficacy and safety of the essential oil-based product in patients with mild to moderate symptomatic COVID-19 Positive infection confirmed by PCR. A computational simulation approach of the molecular interaction (binding) of the main components of essential oils exhibiting antiviral activity with known intracellular protein targets of SARS-CoV-2 (nsp5: Main Protease) was adopted as a rationale for this study. SARS-CoV-2, a single-stranded RNA virus, has four major structural proteins Spike (S), Membrane (M), Envelope glycoprotein (E) and Nucleocapsid (N) protein and non-structural proteins (nsp). These non-structural proteins, of which there are 16 in total in the genome of the virus, play key roles in the mechanisms of the virus life cycle, including replication, transcription, protein synthesis and modification of RNA. Main protease (Main protease, Mpro, 3CLpro), virus Since they are directly involved in the maturation of these nsp proteins, which have an important role in many mechanisms of the life cycle, they have been the target enzyme in the development of new antiviral drugs for the treatment of COVID-19. In this study, our main rationale is to investigate the effect of essential oils on nsp5: Main Protease enzyme activations.

Participants needed: 280
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Biodex S.AUpdated: Jun 13, 2024Locations: 10
Eligibility criteria

Patients must be between 18<X< 65 years of age. [+3]

Patients < 18 years of age, [+15]

Status: Recruiting

Dynamics of Markers of Infection and Inflammation in Hospitalized Coronavirus Disease 2019 (COVID-19) Patients

Patients requiring admission to the hospital due to a moderate and severe COVID-19 infection may differ in their ability to respond to viral infection and to eliminate viral load. Several comorbidities and interventions like antivirotic or antiinflammatory treatment may also modify expected patients response and decrease of viral load. In this observational study, evolution of selected inflammatory markers, indicators of severity of infection and patient characteristics will be followed and recorded in hospitalized patients with COVID-19.

Participants needed: 30
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: University Hospital Hradec KraloveUpdated: May 10, 2024Locations: 1
Eligibility criteria

SARS CoV2 positive test within last 14 day [+2]

known history of intersticial lung disease [+1]