NCT05734365 COPD-ICU Multicentre Prospective Observational Register
| NCT ID | NCT05734365 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Versailles Hospital |
| Condition | COPD Exacerbation Acute |
| Study Type | OBSERVATIONAL |
| Enrollment | 500 participants |
| Start Date | 2022-11-01 |
| Primary Completion | 2027-12 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 500 participants in total. It began in 2022-11-01 with a primary completion date of 2027-12.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
COPD is one of the leading causes of morbidity, mortality and health care utilisation worldwide. Currently, COPD is the third leading cause of death worldwide and is therefore a major public health problem. Projections show an increase in the prevalence and burden of COPD in the coming decades due to ageing populations and continued exposure to risk factors. In patients with COPD, mortality due to exacerbations is about 35%. Exacerbations represent the most important respiratory event in the history of this chronic disease and are of major socio-economic interest (about 50-75% of healthcare expenditure in this disease). In the most severe cases, COPD exacerbations lead to respiratory distress with hypercapnic ventilatory acidosis requiring ventilatory support. These most severe episodes are common, accounting for 20% of exacerbations and are a signal of advanced disease, with a high risk of future hospitalisations and a limited long-term prognosis. Despite progress in management, the mortality of these severe acute exacerbations is around 15% in the ICU and 20% in hospital. The long-term prognosis following hospitalisation for an acute exacerbation of COPD is poor with a 5-year mortality of around 50%. On the one hand, the means and treatments likely to improve the prognosis of these patients are of great medical and socio-economic interest, on the other hand, it seems important to identify the elements that may be associated with management failure and to treat them where appropriate. Thus, improving scientific knowledge thanks to prospective data, evaluating the different characteristics and prognosis of patients hospitalised for a severe acute exacerbation of COPD seems, in the 21st century, a major axis in order to continue to optimise the individual management of these patients but also collectively, given the COPD public health burden.
Eligibility Criteria
Inclusion Criteria: 1. Age ≥ 40 years old 2. COPD documented or strongly suspected * Chronic respiratory symptoms (dyspnoea, cough and/or sputum) * Exposure to a known risk factor for COPD (such as tobacco smoke) * If available, respiratory function tests showing non- or partially reversible obstructive syndrome (post-bronchodilator ratio FEV1/CV \< 0.7) 3. Severe acute exacerbation, defined as a worsening of the patient's usual respiratory symptoms with signs of acute respiratory distress (polypnoea ≥ 30 cycles.min-1 or use of accessory respiratory muscles) and/or hypercapnic acidosis (with PaCO2 ≥ 45 mmHg and pH ≤ 7.35) 4. Admission to an ICU, or a dedicated respiratory intensive care unit Exclusion Criteria: 1. Known asthma (according to the criteria of the international "Global Initiative for Asthma" guidelines) 2. Patient refusal to participate (information note, application for non-opposition)
Contact & Investigator
Alexis Ferré, MD
PRINCIPAL INVESTIGATOR
Centre hospitalier de Versailles, 78150, Le Chesnay
Frequently Asked Questions
Who can join the NCT05734365 clinical trial?
This trial is open to participants of all sexes, aged 40 Years or older, studying COPD Exacerbation Acute. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05734365 currently recruiting?
Yes, NCT05734365 is actively recruiting participants. Contact the research team at aferre@ght78sud.fr for enrollment information.
Where is the NCT05734365 trial being conducted?
This trial is being conducted at Le Chesnay, France.
Who is sponsoring the NCT05734365 clinical trial?
NCT05734365 is sponsored by Versailles Hospital. The principal investigator is Alexis Ferré, MD at Centre hospitalier de Versailles, 78150, Le Chesnay. The trial plans to enroll 500 participants.
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