RECRUITING

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.

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Blood-based Biomarkers of Acute Lung Injury/Acute Respiratory Distress Syndrome

Quick Facts

Study Start:2025-05-20
Study Completion:2026-11-20
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07125079

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Shampa Chatterjee, PhD
CONTACT
215-898-9101
shampac@pennmedicine.upenn.edu
Christian Bermudez, MD
CONTACT
215-615-5864
christian.bermudez@pennmedicine.upenn.edu

Principal Investigator

Shampa Chatterjee, PhD
PRINCIPAL_INVESTIGATOR
University of Pennsylvania
Christian Bermudez, MD
PRINCIPAL_INVESTIGATOR
University of Pennsylvania
Asad Usman, MD
STUDY_DIRECTOR
University of Pennsylvania

Study Locations (Sites)

Hospital Of the University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States

Collaborators and Investigators

Sponsor: University of Pennsylvania

  • Shampa Chatterjee, PhD, PRINCIPAL_INVESTIGATOR, University of Pennsylvania
  • Christian Bermudez, MD, PRINCIPAL_INVESTIGATOR, University of Pennsylvania
  • Asad Usman, MD, STUDY_DIRECTOR, University of Pennsylvania

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-20
Study Completion Date2026-11-20

Study Record Updates

Study Start Date2025-05-20
Study Completion Date2026-11-20

Terms related to this study

Keywords Provided by Researchers

  • ROS
  • ARDS
  • PIP-2
  • immune cells
  • peripheral blood mononuclear cells

Additional Relevant MeSH Terms

  • ARDS (Acute Respiratory Distress Syndrome)