Non-invasive Ventilation or CPAP in OSA-COPD Following Admission for an Acute Hypercapnic Respiratory Failure

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-84
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Chronic obstructive pulmonary disease (COPD) is a major public health problem with 212.3 million prevalent cases of COPD worldwide and 3.3 million deaths related to COPD in 2019. Obstructive sleep apnoea (OSA) is the most common sleep disordered breathing. It is estimated that almost 1 billion adults have OSA worldwide.

Given the increasing prevalence of obesity, co-morbid OSA is frequently seen in patients with COPD. Co-morbid OSA has been shown to increase mortality, to reduce quality of life and to favour acute exacerbation of COPD. For those admitted for a life-threatening exacerbation of COPD requiring an intensive care admission for acute hypercapnic failure, they are more likely to get readmitted. For those admitted for an acute exacerbation in any ward, they are more likely to be re-admitted for another exacerbation within 180-days if their OSA is not treated.

Unfortunately, data regarding the best management of OSA in patients with co-morbid COPD are lacking as they were often excluded from clinical trials involving patients with COPD. Therefore, CPAP or NIV are administered without scientific evidence establishing which treatment is the most appropriate.

Eligibility criteria

Qualifiers

Age ≥ 18 and < 85 years

Patient with a diagnosis of COPD according to GOLD guidelines

Patient admitted for an acute exacerbation of COPD requiring acute NIV or invasive ventilation or high-flow therapy (pH <7.35 with PaCO2 >45mmHg/6kPa)

Patient that has been weaned from acute NIV or invasive ventilation or high flow therapy

Disqualifiers

Patient with NIV treatment

Patients who decline any use of NIV or CPAP in the home setting

Significant psychiatric disorder or dementia that would prevent adherence to study protocol

Tobacco use <10 pack-year

Trial design

Treatments tested in this trial

  • Non-invasive Ventilation (NIV)
  • Continous Positive Airway Pressure (CPAP)

Treatment groups

386 Participants
are divided into 2 treatment groups