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Consolidated Standards of Reporting Trials (CONSORT) diagram of patients enrolled in the study. #: Two pre-screen/screen failures were erroneously randomised,

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Presentation on theme: "Consolidated Standards of Reporting Trials (CONSORT) diagram of patients enrolled in the study. #: Two pre-screen/screen failures were erroneously randomised,"— Presentation transcript:

1 Consolidated Standards of Reporting Trials (CONSORT) diagram of patients enrolled in the study. #: Two pre-screen/screen failures were erroneously randomised, one to each study arm. Consolidated Standards of Reporting Trials (CONSORT) diagram of patients enrolled in the study. #: Two pre-screen/screen failures were erroneously randomised, one to each study arm. They were subsequently excluded from the intent-to-treat (ITT) population, as they did not receive a dose of study medication. A further patient was excluded from the ITT population due to a protocol deviation. UMEC: umeclidinium; GLYCO: glycopyrronium; 24H: subset of patients who completed 24-h spirometry on day 1 and day 84; COPD: chronic obstructive pulmonary disease. Tara Rheault et al. ERJ Open Res 2016;2: ©2016 by European Respiratory Society


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