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Clinical Research Directory

Browse clinical research sites, groups, and studies.

4 clinical studies listed.

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Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)

Tundra lists 4 Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS) clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT06513949

Anti-CD14 Treatment With IC14 in Hospitalized ARDS Patients

Hospitalized patients with ARDS will be randomized to intravenous treatment with a monoclonal antibody against CD14, called IC14, or placebo. They will be followed for 28 days. The primary outcome is the day 4 oxygenation index assessed as a continuous measure.

Gender: All

Ages: 18 Years - Any

Updated: 2025-08-20

1 state

Acute Respiratory Distress Syndrome
Adult Respiratory Distress Syndrome
Acute Lung Injury
+1
RECRUITING

NCT06123962

ALI/ARDS Clinical Sub-phenotyping Study

1. Construct a structured clinical data and biosample information platform for Chinese patients with acute lung injury/ acute respiratory distress syndrome. 2. By deciphering the heterogeneity of patients with acute lung injury/ acute respiratory distress syndrome, achieve clinical, longitudinal physiological, and biological sub-phenotyping to guide individualized precision treatment and improve prognosis.

Gender: All

Ages: 18 Years - Any

Updated: 2025-02-12

Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)
RECRUITING

NCT06805409

VExUS in Ards Patients and Association with AKI

A single-center prospective observational study will be conducted with the aim of determining the prevalence of venous congestion during ARDS using venous Doppler and the VExUS score.

Gender: All

Ages: 18 Years - 100 Years

Updated: 2025-02-03

1 state

Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)
RECRUITING

NCT05002478

Infants with Severe Acute Respiratory Distress Syndrome: the Prone Trial

The main objective is to determine the short-term effect of prone positioning in infants with infection-associated severe acute respiratory distress syndrome. The investigators compare oxygenation parameters and measurements from electrical impedance tomography (EIT) and lung ultrasonography (LUS) in mechanically ventilated infants in prone position versus supine position after surfactant administration.

Gender: All

Ages: Any - 12 Months

Updated: 2024-11-20

Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)
Surfactant Dysfunction
Infant