Status:

COMPLETED

A Retrospective rEal-life daTa Study to Assess the exaceRbations and Lung functIon in Chronic Obstructive Pulmonary Disease ( COPD ) patiEnts receiVing Fluticasone/Salmeterol Comparing to Those Εscalating in Open-triple Fluticasone/Salmeterol, Long Acting Muscarinic Antagonist (LAMA) Combination

Lead Sponsor:

Elpen Pharmaceutical Co. Inc.

Conditions:

COPD

COPD Exacerbation

Eligibility:

All Genders

18-80 years

Brief Summary

Inhaled corticosteroid (ICS)/long-acting β2-agonist (LABA) combination is commonly prescribed to treat COPD; we will perform a retrospective analysis on the effect of adding a long-acting muscarinic r...

Detailed Description

According to the current guidelines for the treatment of COPD, it is recommended to use combination therapies with different or complementary mechanisms of action . Data suggest that open triple thera...

Eligibility Criteria

Inclusion

  • Inclusion
  • Patients with COPD who started treatment with a fixed combination of fluticasone / salmeterol via the Elpenhaler® device after 01/01/2012 and were treated continuously for at least 1 year during the recording period.
  • Patients for whom spirometric data are available per monitoring year during recording.
  • Patients for whom exacerbation data are available per monitoring year during recording.
  • Exclusion
  • •Patients with asthma

Exclusion

    Key Trial Info

    Start Date :

    May 1 2019

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ACTUAL

    End Date :

    December 31 2019

    Estimated Enrollment :

    1000 Patients enrolled

    Trial Details

    Trial ID

    NCT03858348

    Start Date

    May 1 2019

    End Date

    December 31 2019

    Last Update

    February 20 2024

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    Papanikolaou Hospital of Thessaloniki

    Thessaloniki, Greece