Objective: To characterize FeNO levels that may be indicative of eosinophilic airway inflammation in patients with chronic obstructive airways disease Number of participants: Approximately 200 subjects will be enrolled Reference product: NIOX MINO® Instrument (09-1100) Performance assessments: Fractional Exhaled Nitric Oxide (FeNO) Measurements will be performed according to the "Perform FeNO Measurement" guidelines on page 7 of the NIOX MINO® User Manual Safety assessments: The Investigator is responsible for the detection, reporting, and documentation of events meeting the definition of an Adverse Event (AE) and/or Serious Injuries as provided in this clinical investigation plan from the time that informed consent has been provided and during the study period Criteria for evaluations: This is an observational, pilot study and there are currently no plans for a formal statistical analysis. Information gained from this study may used to design subsequent studies in patients with chronic obstructive airways disease. Information collected will be summarized in a clinical study report but will not be subject to formal hypothesis testing
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Spirometry Results: FEV1 (L)
Timeframe: Single Visit
Spirometry Results: FVC (L)
Timeframe: Single Visit
Spirometry Results: FEV1 (% Predicted)
Timeframe: Single Visit
Spirometry Results: FEF50% (L/Sec)
Timeframe: Single Visit
Spirometry Results: FEF25-75 (L/Sec)
Timeframe: Single Visit
Spirometry Results: PEF (L/Min)
Timeframe: Single Visit
FeNO Levels by GOLD Stage of Severity
Timeframe: Single Visit
FeNO Levels by Inhaled Corticosteroid Use
Timeframe: Single Visit
FeNO Levels by Smoking Status
Timeframe: Single Visit
FeNO Levels by ICD 9 Code Category
Timeframe: Single Visit
Mean FeNO Levels by ICD 9 Code Category
Timeframe: Single Visit