Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT03859050

Alveolar Macrophage Programming Following Endotoxin Exposure

Led by National Jewish Health · Updated on 2025-05-06

25

Participants Needed

1

Research Sites

693 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The histologic hallmarks of lung inflammation include 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).

CONDITIONS

Official Title

Alveolar Macrophage Programming Following Endotoxin Exposure

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Written, informed consent
  • Age between 18 and 50 years
Not Eligible

You will not qualify if you...

  • Current or recent illness within the past 2 weeks
  • Presence or prior history of cardiac, pulmonary, or systemic disease
  • Bleeding disorder or use of systemic anticoagulants or antiplatelet therapy
  • American Society of Anesthesiology (ASA) class 2 or greater
  • Immunocompromised state including HIV, immunoglobulin deficiency, or use of systemic immunosuppressants
  • Use of inhaled substances including tobacco, marijuana, e-cigarettes, cocaine, methamphetamines, or toxic vapors in the past 3 months or a smoking history greater than 10 pack-years
  • Alcohol use disorder or more than 7 drinks per week for women or more than 14 drinks per week for men in the past 3 months
  • Allergy or prior adverse reaction to lidocaine, midazolam, or fentanyl
  • Abnormal spirometry or electrocardiogram at screening
  • Pregnant or breastfeeding

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

National Jewish Health

Denver, Colorado, United States, 80206

Actively Recruiting

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Research Team

K

Kara Mould

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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