Actively Recruiting

Age: 21Years - 90Years
All Genders
NCT07125079

Lung Injury is One of the Primary Causes of Morbidity and Mortality in Critically Ill Patients. These Patients Will be Monitored for: 1) Immune Cell Activation 2) Blood-based Biomarkers. In Vitro Models Derived From These Samples Will be Treated With Novel Agent PIP-2 to Evaluate Its Efficacy.

Led by University of Pennsylvania · Updated on 2025-08-15

36

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

Sponsors

U

University of Pennsylvania

Lead Sponsor

P

Peroxitech Inc

Collaborating Sponsor

AI-Summary

What this Trial Is About

Acute Lung Injury (ALI) and Acute Respiratory Distress Syndrome (ARDS) is a condition where high levels of inflammation damage the lung. This is a highly morbid condition with no specific pharmacologic therapies. The investigators posit that ARDS is caused due to an exaggerated activation of immune cells and that blockade of this activation may reduce lung damage/injury and help in ARDS management and possibly recovery. To test this hypothesis, the investigators propose to generate an in vitro immune cell model and test a novel (reactive oxygen species) blocking agent PIP-2 on this model. The investigating team will obtain blood of ARDS patients and isolate immune cells (specifically peripheral blood mononuclear cells or PBMC) and monitor the activation of these cells and their blockade by PIP-2. This is entirely an in vitro study.

CONDITIONS

Official Title

Lung Injury is One of the Primary Causes of Morbidity and Mortality in Critically Ill Patients. These Patients Will be Monitored for: 1) Immune Cell Activation 2) Blood-based Biomarkers. In Vitro Models Derived From These Samples Will be Treated With Novel Agent PIP-2 to Evaluate Its Efficacy.

Who Can Participate

Age: 21Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ARDS patients with mild, moderate, or severe ARDS based on PaO2/FiO2 levels ranging from 100 to 300 mmHg
Not Eligible

You will not qualify if you...

  • Pregnant women
  • Children

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital Of the University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

S

Shampa Chatterjee, PhD

CONTACT

C

Christian Bermudez, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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