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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02552160
Other study ID # D6570R00001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 24, 2015
Est. completion date December 31, 2017

Study information

Verified date December 2018
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Prospective, multi-centre, non-interventional study to collect findings about the effects of LABA/LAMA (Long Acting Beta2-Agonists / Long Acting Muscarinic Antagonists) combination preparations on COPD (Chronic obstructive pulmonary disease) symptoms and quality of life under real conditions and to find out what types of patients are selected for this therapy by physicians.


Description:

Retrospective aspect of documentation: For patients who have already been changed over to a fixed-dose combination, lung function parameters and CAT (COPD Assessment Test™) score from the time prior to the changeover will be documented.


Recruitment information / eligibility

Status Completed
Enrollment 3732
Est. completion date December 31, 2017
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Female/male of at least 40 years of age

- Patient diagnosed with COPD

- Patient was changed over within the last 3 months to a fixed-dose combination (FDC) (Aclidinium/Formeterol, Glycopyrronium/Indacaterol or Umeclidinium/Vilanterol), or there is already the intent to change the patient over to a fixed-dose combination (Aclidinium/Formeterol, Glycopyrronium/Indacaterol or Umeclidinium/Vilanterol).

- Lung function parameters and CAT score from the time prior to the changeover to an FDC are on record (within the last 6 months in the case of patients who have already been changed over) or are determined at the 1st visit (in the case of patients who have not yet been changed over but for whom such a changeover is intended).

- Signed declaration of consent

Exclusion Criteria:

- The prescribing information for the fixed-dose combinations (Duaklir® Genuair®, Ulibtro® Breezhaler® or Anoro®) list contraindications for the patient.

- Patient is pregnant, plans to become pregnant, or is nursing during the therapy period.

- Patient suffers from hypersensitivity to one of the active ingredients of the fixed-dose combinations.

- Patient is participating in a clinical trial.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Research Site Aachen D6570r00001
Germany Research Site Aldenhofen D6570r00001
Germany Research Site Aldenhoven D6570r00001
Germany Research Site Alzey D6570r00001
Germany Research Site Ansbach D6570r00001
Germany Research Site Apolda D6570r00001
Germany Research Site Aschau D6570r00001
Germany Research Site Auerbach D6570r00001
Germany Research Site Augsburg D6570r00001
Germany Research Site Bad Fallingbostel D6570r00001
Germany Research Site Bad Hersfeld D6570r00001
Germany Research Site Bad Honnef D6570r00001
Germany Research Site Bad Lippspringe D6570r00001
Germany Research Site Bad Reichenhall D6570r00001
Germany Research Site Bad Sachsa D6570r00001
Germany Research Site Bad Windsheim D6570r00001
Germany Research Site Bad Woerishofen D6570r00001
Germany Research Site Bamberg D6570r00001
Germany Research Site Beelitz-Heilstaetten D6570r00001
Germany Research Site Bergisch Gladbach D6570r00001
Germany Research Site Berlin D6570r00001
Germany Research Site Biberach D6570r00001
Germany Research Site Birkenwerder D6570r00001
Germany Research Site Bitterfeld-Wolfen D6570r00001
Germany Research Site Bochum D6570r00001
Germany Research Site Boehlen D6570r00001
Germany Research Site Bonn D6570r00001
Germany Research Site Bottrop D6570r00001
Germany Research Site Braunschweig D6570r00001
Germany Research Site Bruchsal D6570r00001
Germany Research Site Buechen D6570r00001
Germany Research Site Burghaslach D6570r00001
Germany Research Site Burgwedel D6570r00001
Germany Research Site Celle D6570r00001
Germany Research Site Chemnitz D6570r00001
Germany Research Site Cottbus D6570r00001
Germany Research Site Darmstadt D6570r00001
Germany Research Site Delitzsch D6570r00001
Germany Research Site Dessau D6570r00001
Germany Research Site Dorsten D6570r00001
Germany Research Site Dortmund D6570r00001
Germany Research Site Dresden D6570r00001
Germany Research Site Dueren D6570r00001
Germany Research Site Duesseldorf D6570r00001
Germany Research Site Duisburg D6570r00001
Germany Research Site Eimsheim D6570r00001
Germany Research Site Ellerstadt D6570r00001
Germany Research Site Elsterwerda D6570r00001
Germany Research Site Elterlein D6570r00001
Germany Research Site Essen D6570r00001
Germany Research Site Euerbach-Obbach D6570r00001
Germany Research Site Euskirchen D6570r00001
Germany Research Site Flensburg D6570r00001
Germany Research Site Frankfurt D6570r00001
Germany Research Site Frankfurt/M. D6570r00001
Germany Research Site Freiberg D6570r00001
Germany Research Site Fuerstenwalde D6570r00001
Germany Research Site Fuerth D6570r00001
Germany Research Site Ganderkesee D6570r00001
Germany Research Site Garching D6570r00001
Germany Research Site Garmisch-Partenkirchen D6570r00001
Germany Research Site Gauting D6570r00001
Germany Research Site Gera D6570r00001
Germany Research Site Gerwisch D6570r00001
Germany Research Site Glienicke D6570r00001
Germany Research Site Greiz D6570r00001
Germany Research Site Guetersloh D6570r00001
Germany Research Site Hagen D6570r00001
Germany Research Site Halberstadt D6570r00001
Germany Research Site Halle D6570r00001
Germany Research Site Hamburg D6570r00001
Germany Research Site Hannover D6570r00001
Germany Research Site Hartenstein D6570r00001
Germany Research Site Heidelberg D6570r00001
Germany Research Site Hemmingen D6570r00001
Germany Research Site Hettstedt D6570r00001
Germany Research Site Hoechstadt D6570r00001
Germany Research Site Hoyerswerda D6570r00001
Germany Research Site Ibbenbueren D6570r00001
Germany Research Site Ingolstadt D6570r00001
Germany Research Site Iserlohn D6570r00001
Germany Research Site Issum D6570r00001
Germany Research Site Jena D6570r00001
Germany Research Site Karlsruhe D6570r00001
Germany Research Site Kevelaer D6570r00001
Germany Research Site Kleve D6570r00001
Germany Research Site Koeln D6570r00001
Germany Research Site Koeln-Hoehenberg D6570r00001
Germany Research Site Koeln-Rodenkirchen D6570r00001
Germany Research Site Koethen D6570r00001
Germany Research Site Kolbermoor D6570r00001
Germany Research Site Krefeld D6570r00001
Germany Research Site Kronach D6570r00001
Germany Research Site Kyritz D6570r00001
Germany Research Site Langenfeld D6570r00001
Germany Research Site Leer D6570r00001
Germany Research Site Leipzig D6570r00001
Germany Research Site Leonberg D6570r00001
Germany Research Site Lippstadt D6570r00001
Germany Research Site Ludwigsburg-Ossweil D6570r00001
Germany Research Site Ludwigshafen D6570r00001
Germany Research Site Luebeck D6570r00001
Germany Research Site Magdeburg D6570r00001
Germany Research Site Mainz D6570r00001
Germany Research Site Mannheim D6570r00001
Germany Research Site Marburg D6570r00001
Germany Research Site Markt Bibart D6570r00001
Germany Research Site Menden D6570r00001
Germany Research Site Merzig D6570r00001
Germany Research Site Moenchengladbach D6570r00001
Germany Research Site Moers D6570r00001
Germany Research Site Monheim D6570r00001
Germany Research Site Mosbach D6570r00001
Germany Research Site Muehlhausen D6570r00001
Germany Research Site Muenchen D6570r00001
Germany Research Site Neumarkt D6570r00001
Germany Research Site Neunkirchen D6570r00001
Germany Research Site Neuruppin D6570r00001
Germany Research Site Neusaess D6570r00001
Germany Research Site Neustadt/Aisch D6570r00001
Germany Research Site Neuwied D6570r00001
Germany Research Site Nuernberg D6570r00001
Germany Research Site Oettingen D6570r00001
Germany Research Site Oschatz D6570r00001
Germany Research Site Oy-Mittelberg D6570r00001
Germany Research Site Pirmasens D6570r00001
Germany Research Site Potsdam D6570r00001
Germany Research Site Pulheim-Braunweiler D6570r00001
Germany Research Site Radebeul D6570r00001
Germany Research Site Rastatt D6570r00001
Germany Research Site Rathenow D6570r00001
Germany Research Site Recklinghausen D6570r00001
Germany Research Site Remscheid D6570r00001
Germany Research Site Reutlingen D6570r00001
Germany Research Site Rosenheim D6570r00001
Germany Research Site Rostock D6570r00001
Germany Research Site Roth D6570r00001
Germany Research Site Ruedersdorf D6570r00001
Germany Research Site Ruesselsheim D6570r00001
Germany Research Site Rust D6570r00001
Germany Research Site Saalfeld D6570r00001
Germany Research Site Saarbruecken D6570r00001
Germany Research Site Saarlouis D6570r00001
Germany Research Site Schleswig D6570r00001
Germany Research Site Schmoelln D6570r00001
Germany Research Site Schoenbrunn D6570r00001
Germany Research Site Schwedt D6570r00001
Germany Research Site Siegen D6570r00001
Germany Research Site Simmern D6570r00001
Germany Research Site Solingen D6570r00001
Germany Research Site Sonsbeck D6570r00001
Germany Research Site Spiesen D6570r00001
Germany Research Site Spremberg D6570r00001
Germany Research Site Steinhagen D6570r00001
Germany Research Site Strasskirchen D6570r00001
Germany Research Site Strausberg D6570r00001
Germany Research Site Stuttgart D6570r00001
Germany Research Site Sulzberg D6570r00001
Germany Research Site Teterow D6570r00001
Germany Research Site Teuchern D6570r00001
Germany Research Site Thaleischweiler-Froeschen D6570r00001
Germany Research Site Trier D6570r00001
Germany Research Site Ulm D6570r00001
Germany Research Site Unterwellenborn D6570r00001
Germany Research Site Ursensollen D6570r00001
Germany Research Site Voerde D6570r00001
Germany Research Site Wallenhorst D6570r00001
Germany Research Site Wardenburg D6570r00001
Germany Research Site Waren D6570r00001
Germany Research Site Warendorf D6570r00001
Germany Research Site Wehrheim D6570r00001
Germany Research Site Weilheim D6570r00001
Germany Research Site Weissenburg D6570r00001
Germany Research Site Weisswasser D6570r00001
Germany Research Site Wiesbaden D6570r00001
Germany Research Site Witten D6570r00001
Germany Research Site Wittenberg D6570r00001
Germany Research Site Worms D6570r00001
Germany Research Site Wuppertal D6570r00001
Germany Research Site Zwoenitz D6570r00001

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lung function Assessment of FEV1 (Forced Expiratory Volume), FVC (Forced Vital Capacity) First visit (baseline)
Primary Number of patients with concomitant diseases classified by diagnostic subgroups First visit (baseline)
Primary Number of patients receiving concomitant COPD (Chronic obstructive pulmonary disease) medication classified by therapeutic subgroups First visit (baseline)
Primary Number of patients with exacerbations within the previous 24 months History of previous exacerbations that will be collected at first observational visit. First visit (baseline)
Secondary Change in well-being and quality of life CAT (COPD Assessment Test™) questionnaire will be completed at each visit, approximately every 3 months. First visit (baseline) to end of observational period at 12 months
Secondary Effect on the severity of the shortness of breath mMRC (modified Medical Research Council Dyspnea Scale) questionnaire will be completed at each visit, approximately every 3 months. First visit (baseline) to end of observational period at 12 months
Secondary Change in the night-time and early-morning COPD symptoms NiSCI/EMSCI (Night-time symptoms of COPD Instrument / Early-morning symptoms of COPD instrument) questionnaire will be completed at each visit, approximately every 3 months. First visit (baseline) to end of observational period at 12 months
Secondary Lung function Assessment of FEV1, FVC at each visit, approximately every 3 months. First visit (baseline) to end of observational period at 12 months
Secondary Number of exacerbations by grade Number of exacerbations will be collected at each visit, approximately every 3 months First visit (baseline) to end of observational period at 12 months
Secondary Adverse events Adverse events will be collected at each visit, approximately every 3 months. First visit (baseline) to end of observational period at 12 months
Secondary Handling of inhaler Questionnaire regarding handling of inhaler by patient At 12 months
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