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Phase 4 Completed N=18 Randomized Double-blind Treatment

A Proof of Concept Study to Evaluate the Dose Response for the Systemic Benefit Risk Ratio of Inhaled Fluticasone Propionate in Chronic Obstructive Pulmonary Disease

Source: ClinicalTrials.gov NCT00995475 ↗
Enrolled (actual)
18
Serious AEs
0.0%
Results posted
Apr 2019
Primary outcomePrimary: CRP — 2.9; 2.0 mg/L
◆ Published Evidence
Emerging
15citations · ~1 / year
Dose-response for inhaled fluticasone on airway and systemic inflammation in COPD.
The European respiratory journal · 2011 · Open access · High-confidence link

Summary

Chronic Obstructive Pulmonary Disease (COPD) is a major worldwide problem.Steroids inhalers are now an established treatment for COPD. Inhaled steroids can have a number of bad effects including suppression of the adrenal glands because of absorption. A previous study in patients with COPD. C-reactive Protein (CRP) is a peptide produced in the liver in response to inflammation. Elevated circulating levels of CRP are associated with heart conditions. High levels of CRP have also been found in patients with COPD. In some studies, steroid inhalers have reduced CRP levels, and that of other inflammatory mediators, in patients with COPD. It is unknown whether this reflects a reduction in lung inflammation or an effect of systemically absorbed corticosteroid. It is proposed to investigate the link between inhaled corticosteroid and serum CRP, lung inflammation (measured by exhaled nitric oxide) and systemic absorption of steroids.

Linked Publications

  • Dose-response for inhaled fluticasone on airway and systemic inflammation in COPD.
    The European respiratory journal · 2011 · 15 citations · Open access · High-confidence link

Outcome Measures

OutcomeResultp-value
PRIMARY
CRP
2.9; 2.0
SECONDARY
Alveolar Nitric Oxide
1.7; 3.1
SECONDARY
OUCC
2.7; 8.8

Eligibility Criteria

Inclusion Criteria

  • Current or ex-smokers
  • Aged over 50years
  • FEV1/FVC ratio <0.7
  • FEV1<80% predicted
  • Improvement in FEV1 following short acting beta-agonist not greater than 15% and 200ml.

Exclusion Criteria

  • Diagnosis of asthma, bronchiectasis or ABPA
  • Inability to perform study procedures or give informed consent
  • Known sensitivity to trial medications
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00995475) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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