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Completed

NCT Number: NCT02557958

Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study

Chronic Obstructive Pulmonary Disease Transcription Factor and Cytokine Study.

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Key information

About this study

Chronic Obstructive Pulmonary Disease (COPD) is the 4th leading cause of death in the United States. It is projected to be the leading cause of death by 2020. As many as 24 million Americans are estimated to suffer from impaired lung function. Of those more than 12 million were actually diagnosed with COPD, and over 118,000 deaths were attributed to COPD in 2004.

COPD has been linked with an increased risk for lung cancer. Both airway obstruction, defined by abnormal pulmonary function tests (PFTs), and CT scan diagnosed emphysema were shown to be independent risk factors for lung cancer.

Treatment for COPD includes cessation of environmental exposures (i.e. smoking), dampening the inflammatory response, symptoms control and, for a small subgroup, surgical approaches and lung transplant. Nevertheless, the effectiveness of these treatment options to change the natural history of this disease is very limited. Recent evidence suggests a new role for macrolides as immune-modulators in patients with COPD, although the mechanisms are not clearly determined.

The investigators hypothesize that in patients with COPD, treatment with azithromycin will show reduced inflammatory markers, transcription factors changes, and lung function changes consistent with reduced inflammation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • Key Inclusion Criteria: List primary criteria for study inclusion (i.e. do not need to enter entire list of inclusion criteria).
  • Patient must be 50 years old or older.
  • Patient must have a smoking history of at least 20 pack-years
  • Patient must have stable COPD, GOLD 0, I and/or IIA.
  • CT of chest with evidence of emphysema
  • Key Exclusion Criteria: List primary criteria for study exclusion (i.e. do not need to enter entire list of inclusion criteria).
  • FEV1 < 70%.
  • Exacerbations (defined as use of oral steroids or antibiotics) in the previous month.
  • Cardiovascular Disease defined as abnormal EKG, known or suspected coronary artery disease or congestive heart failure.
  • Diabetes mellitus
  • Renal disease
  • Liver disease
  • Lung cancer
  • ETOH use of more than >6 beers >4 mixed drinks daily

Treatment and study plan

Azithromycin

Drug

We hypothesize that in patients with COPD, treatment with azithromycin will show reduced inflammatory markers, transcription factors changes, and lung function changes consistent with reduced inflammation.

Other names: Zithromax

Placebo

Drug

We hypothesize that in patients with COPD, treatment with placebo will show NO change in inflammatory markers, transcription factor changes and lung function from baseline.

Primary outcomes

  1. Inflammatory markers

    Time frame: outcome will be assessed up to two months post initial bronchoscopy

    Cytokines in BAL in pg/mL

Secondary outcomes

  1. transcription factor changes

    Time frame: outcome will be assessed up to two months post initial bronchoscopy

    BAL cell differential in percentage

  2. Lung function changes

    Time frame: outcome will be assessed up to two months post initial bronchoscopy

    Forced Vital Capacity (FVC)

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Registry information

Important dates

Study start
2009
Primary completion
2018
Study completion
2018
First posted
Sep 23, 2015
Registry last updated
Mar 21, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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