Skip to content

Macrophage Programing in Acute Lung Injury

Macrophage Programing in Acute Lung Injury

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03844893
Enrollment
56
Registered
2019-02-19
Start date
2019-10-31
Completion date
2023-03-31
Last updated
2019-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome

Brief summary

The histologic hallmarks of lung inflammation and in the extreme, acute respiratory distress syndrome (ARDS), include intense accumulation of inflammatory cells in the airspaces and interstitium, injury to alveolar epithelial and endothelial cells, loss of epithelial-capillary integrity and accumulation of edema fluid in the interstitium and airspaces. Accordingly, for alveolar repair to occur inflammation must be halted, debris and inflammatory cells removed, injured tissue cells replaced, and capillary barrier function re-established. Macrophages are key players in all of these. Here the investigators hypothesize that resident alveolar macrophages and recruited macrophages serve completely different functions, acting independently (i.e. division of labor) yet cooperatively (synergism).

Interventions

PROCEDUREMini bal

Mini-BAL is a minimally invasive technique frequently used in the investigator's local intensive care units (ICUs) to obtain alveolar fluid samples from mechanically ventilated patients. This is typically done for microbial analysis.

Sponsors

National Jewish Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Written, informed consent (by surrogate if unconscious or if altered mental status) 2. Admission to a Medical Intensive care unit 3. Orally/nasally intubated, evaluable within 24 h of intubation or onset of ARDS 4. Expected to remain mechanically ventilated for at least 48 h after the first study procedure.

Exclusion criteria

1. Treatment with immunosuppressants in the prior 3 months (antineoplastic agents, tumor necrosis factor alpha antagonists, cyclosporine, methotrexate, azathioprine, or mycophenolate. Treatment with glucocorticoids for septic shock is acceptable). 2. History of solid organ or bone marrow transplantation 3. History of chronic lung disease (e.g. COPD, pulmonary fibrosis, cystic fibrosis) 4. Human immunodeficiency virus positivity 5. Severe or massive hemoptysis 6. At significant risk for bleeding (INR \> 3 or PTT \> 3x normal) 7. Presence of an advanced directive to withhold life-sustaining treatment 8. Morbid state or expected to survive less than 14 days because of an advanced co-morbid medical condition; 9. Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Evaluation and roles of macrophages during ARDS10 daysEvaluation of resident alveolar macrophages will be distinguished with flow cytometry and enumerated

Contacts

Primary ContactChristine Griesmer, MPH
griesmerc@njhealth.org303-398-1325

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026