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Search / Trial NCT03954132

Spiolto® Respimat® (Tiotropium/Olodaterol) Versus Triple Combination Therapy in Everyday Clinical Treatment Practice for Chronic Obstructive Pulmonary Disease (EVELUT®)

Launched by BOEHRINGER INGELHEIM · May 15, 2019

Trial Information

Current as of June 24, 2025

Completed

Keywords

ClinConnect Summary

COPD patients on LABA/ICS maintenance therapy with dyspnea (mMRC ≥ 1) and other symptoms (CATTM ≥ 10), who are switched to either Spiolto® Respimat® in the new reusable inhaler or any triple therapy (LAMA + LABA + ICS) as an open or fixed combination according to approved SmPCs at baseline at the discretion of their attending physician.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients can be included if all of the following criteria are met:
  • Diagnosis of COPD
  • Symptomatic (with regard to dyspnea (mMRC Dyspnea score ≥1) AND with regard to symptoms (CAT Score ≥10) at the same time)
  • Patients on LABA/ICS maintenance therapy who are switched to Spiolto® Respimat® in the new reusable inhaler or a free/fixed triple combination of LABA + LAMA + ICS at Visit 1 at the discretion of the treating physician.
  • Adults who are contractually capable and mentally able to understand and follow the instructions of the study personnel
  • Male or female
  • Patients aged ≥40 years of age
  • Written informed consent prior to study participation
  • The patient is willing and able to follow the procedures outlined in the protocol
  • Exclusion Criteria:
  • Patients with contraindications acc. to SmPC
  • Patients not on LABA/ICS maintenance treatment at visit 1, e.g., mono or dual bronchodilation only, ICS only, or a triple combination of LAMA + LABA + ICS (either as a fixed combination product or as separate components)
  • Lack of informed consent
  • Pregnant and/or lactating females
  • Acute exacerbation of COPD (within 4 weeks prior to Visit 1)
  • Frequently exacerbating patients, i. e. patients with ≥2 moderate exacerbations within the last 12 months or ≥1 exacerbation leading to hospitalization within the last 12 months
  • Acute respiratory failure (pH \<7,35 and/ or respiratory rate \>30/min within 3 months prior to Visit 1)
  • History or current diagnosis of asthma
  • History or current diagnosis of asthma-COPD overlap
  • History or current diagnosis of allergic rhinitis within the last 5 years
  • History or current diagnosis of lung cancer within the last 5 years
  • Participation in a parallel interventional clinical trial
  • mild exacerbation: additional use of short-acting bronchodilators and treated by the patient without consulting a physician
  • moderate exacerbation: treatment includes medical prescription of a systemic corticosteroid and/or antibiotic
  • severe exacerbation: exacerbation leading to hospitalization

About Boehringer Ingelheim

Boehringer Ingelheim is a global, research-driven pharmaceutical company dedicated to improving health and quality of life through innovative therapies. Established in 1885 and headquartered in Ingelheim, Germany, the company focuses on the development of prescription medicines in key therapeutic areas, including respiratory diseases, cardiovascular health, oncology, and immunology. Boehringer Ingelheim is committed to advancing medical science through rigorous clinical trials and collaborative research, striving to bring novel treatments to patients while upholding the highest standards of safety and efficacy. With a strong emphasis on sustainability and corporate responsibility, the company aims to make a meaningful impact on global health challenges.

Locations

Stuttgart, , Germany

Darmstadt, , Germany

Bad Wörishofen, , Germany

Berlin, , Germany

Berlin, , Germany

Büchen, , Germany

Duisburg, , Germany

Garmisch Partenkirchen, , Germany

Gelsenkirchen, , Germany

Grafenrheinfeld, , Germany

Halle (Saale), , Germany

Kamp Lintfort, , Germany

Mannheim, , Germany

Münnerstadt, , Germany

Rostock, , Germany

Rüsselsheim, , Germany

Viernheim, , Germany

Weißenburg I Bay, , Germany

Witten, , Germany

Witten, , Germany

Bad Sachsa, , Germany

Bergisch Gladbach, , Germany

Berkatal, , Germany

Berlin, , Germany

Berlin, , Germany

Bonn, , Germany

Breuberg, , Germany

Bruchsal, , Germany

Böhlen B Leipzig, , Germany

Cottbus, , Germany

Deggingen, , Germany

Dortmund, , Germany

Düsseldorf, , Germany

Forchheim , Oberfr, , Germany

Fürstenwalde /Spree, , Germany

Gelsenkirchen, , Germany

Gelsenkirchen, , Germany

Gütersloh, , Germany

Halle (Saale), , Germany

Hamburg, , Germany

Hamburg, , Germany

Heidelberg , Neckar, , Germany

Heilbad Heiligenstadt, , Germany

Ibbenbüren, , Germany

Jerichow, , Germany

Kamen , Westf, , Germany

Koblenz Am Rhein, , Germany

Kronach , Oberfr, , Germany

Köthen (Anhalt), , Germany

Lahnau, , Germany

Leipzig, , Germany

Leipzig, , Germany

Ludwigshafen Am Rhein, , Germany

Ludwigshafen Am Rhein, , Germany

Marburg, , Germany

Menden (Sauerland), , Germany

Mosbach , Baden, , Germany

München, , Germany

Neumarkt I.D.Opf., , Germany

Nürnberg , Mittelfr, , Germany

Nürnberg, , Germany

Oberhausen , Rheinl, , Germany

Potsdam, , Germany

Radebeul, , Germany

Rathenow, , Germany

Schleswig, , Germany

Schweinfurt, , Germany

Seelow, , Germany

Siegen, , Germany

Straubing, , Germany

Strausberg, , Germany

Trier, , Germany

Ulm, Donau, , Germany

Warendorf, , Germany

Wiesbaden, , Germany

Forchheim, Oberfr, , Germany

Heidelberg, Neckar, , Germany

Kamen, Westf, , Germany

Kronach, Oberfr, , Germany

Mosbach, Baden, , Germany

Nürnberg, Mittelfr, , Germany

Oberhausen, Rheinl, , Germany

Patients applied

0 patients applied

Trial Officials

Andrea Marseille, 0049613277141881

Study Chair

andrea.marseille@boehringer-ingelheim.com

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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