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NCT04163536CompletedPhase 3

Comparison of Corticosteroids vs Placebo on Duration of Ventilatory Support During Severe Acute Exacerbations of COPD Patients in the ICU

Comparison of Corticosteroids Versus Placebo on Duration of Ventilatory Support During Severe Acute Exacerbations of COPD Patients in the Intensive Care Unit: a Multicentre Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 23 Oct 2026

Brief summary (registry, in English)

The main objective of this study is to determine if the systemic (intravenous) administration of corticosteroids, as compared to placebo, increases the number of ventilator-free days (VFD) and alive at day 28 in COPD patients admitted to an ICU, a step-up unit or a respiratory care unit for an acute on chronic respiratory failure (ACRF) requiring ventilatory support, either invasive or non-invasive.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
440 (actual)
First submitted
29 Oct 2019
Start date
25 Oct 2021
Primary completion date
24 Nov 2024
Lead sponsor
Versailles Hospital
Diseases
COPD
NCT number
NCT04163536
EU CT number
2024-516651-41-00
EudraCT number
2019-001726-99

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 440
  • From 25 Oct 2021 to the primary completion date, 24 Nov 2024
  • 25 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous diagnostic of asthma ("GINA" international guidelines)
  • Previous inclusion in the present study

Other illness

  • Current and proven active SARS-CoV2 infection
  • Contra-indication of systemic corticosteroids treatment: allergy to corticosteroids, uncontrolled severe arterial hypertension, uncontrolled diabetes mellitus, gastro-intestinal ulcer bleeding
  • Underlying disease requiring chronic daily use of systemic steroids

Other

  • Pneumothorax at inclusion
  • Extracorporeal life support (ECMO or ECCO2R) at inclusion
  • Moribund patient
  • Pregnancy
  • Patients protected by law
  • Exclusion period due to other interventional clinical trial enrolment which can influence primary outcome

Who the study is looking for

  • Patients aged ≥ 40 years
  • Strongly suspected or documented COPD, defined by the presence of the following criterias:
    • Persistent respiratory symptoms (dyspnoea, chronic cough or sputum)
    • History of exposure to a risk factor such as tobacco smoke
    • If available, pulmonary function tests showing airflow limitation not fully reversible (post-bronchodilator ratio of FEV1/ FVC ratio \< 0.7)
  • Severe acute exacerbation, defined by the presence of the two following criteria:
    • COPD exacerbation defined by a change in the patient baseline respiratory symptoms and requiring a change in regular respiratory medication
    • Acute respiratory failure (polypnea ≥ 30 breaths.min-1 or use of accessory respiratory muscles) requiring mechanical ventilation, either invasive or NIV (implemented because of hypercapnic acidosis with PaCO2 ≥ 45 mmHg and pH ≤ 7.35).
  • Admission to an ICU, a step-up unit or a respiratory care unit \<24h
  • Written inform consent from the patient or his surrogates. In patients who are not able to consent on admission an emergency inclusion procedure will be allowed, with a mandatory delayed consent.
  • Affiliation to (or benefit from) French health insurance system.

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (25)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Regional D'Angers
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AngersFranceCompleted
Centre Hospitalier Victor Dupouy
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Argenteuil CedexFranceCompleted
Centre Hospitalier Métropole Savoie
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ChambéryFranceCompleted
Assistance Publique Hopitaux De Paris
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Colombes CedexFranceCompleted
Centre Hospitalier Intercommunal Créteil
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CréteilFranceCompleted
Centre Hospitalier Universitaire de Dijon
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DijonFranceCompleted
Centre Hospitalier Universitaire Grenoble Alpes
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Grenoble Cedex 9FranceCompleted
Centre Hospitalier Departemental Vendee
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La Roche Sur Yon Cedex 9FranceCompleted
Centre Hospitalier De Versailles
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Le Chesnay RocquencourtFranceCompleted
Bicetre Hospital
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Le Kremlin Bicetre CedexFranceCompleted
Centre Hospitalier Le Mans
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Le Mans Cedex 9FranceCompleted
Centre Hospitalier Universitaire De Lille
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Lille CedexFranceCompleted
Hospices Civils De Lyon
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Lyon Cedex 04FranceCompleted
Centre Hospitalier Universitaire de Nantes
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NantesFranceCompleted
Centre Hospitalier Universitaire de Nice
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NiceFranceCompleted
Centre Hospitalier Universitaire D Orleans
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Orleans Cedex 2FranceCompleted
Assistance Publique Hopitaux de Paris
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ParisFranceCompleted
Hopitaux Universitaires Pitie Salpetriere
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Paris Cedex 13FranceCompleted
Centre Hospitalier Universitaire de Poitiers
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PoitiersFranceCompleted
Centre Hospitalier Annecy Genevois
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Pringy CedexFranceCompleted
Centre Hospitalier Universitaire de Rennes
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RennesFranceCompleted
Centre Hospitalier Universitaire Rouen
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Rouen CedexFranceCompleted
Hospital Foch
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SuresnesFranceCompleted
Centre Hospitalier Régional Universitaire de Tours
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ToursFranceCompleted
Centre Hospitalier Bretagne Atlantique
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VannesFranceCompleted

This page is information, not medical advice. Discuss any trial with your doctor.