RecruitingNot ApplicableNCT03890224

Respiratory Support in Chronic Obstructive Pulmonary Disease (COPD) Patients

Respiratory Support in Chronic Obstructive Pulmonary Disease (COPD) Patients After Acute Exacerbation With Monitoring the Quality of Support


Sponsor

Clinact

Enrollment

400 participants

Start Date

Jul 4, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The hypothesis of this study is that any of 3 modalities of home non- invasive ventilation (NIV) compared to 'no NIV' (=hospital NIV) will reduce re-admission to hospital or death in COPD patients who remain persistently hypercapnic following an exacerbation requiring NIV.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • \) Patients with COPD, GOLD C or D and Forced expiratory volume in one second (FEV1)\<65%;
  • \) AHRF (pH\<7,35 and PaCO2≥45mm Hg (≥6kPa) treated more than 24h with Ventilation (non-invasive or invasive);
  • \) 48h to 2 weeks with pH\>7.35, and PaCO2\>45 (\>6kPa) after NIV withdrawal, during daytime at rest without oxygen or ventilatory support (or with O2 if patients are not able to avoid O2 with immediate desaturation below 80%).

Exclusion Criteria16

  • Patient treated with chronic NIV or continuous positive airway pressure (CPAP) device, with ongoing treatment;
  • Primary diagnosis of restrictive lung disease causing hypercapnia i.e. obesity hypoventilation and chest wall disease, however these patients will be included if the "FEV1/Forced vital capacity (FVC)" ratio is \<60% and the FEV1 \<50% if the predominant defect is considered to be obstructive by the center clinician;
  • BMI \> 35 kg/m2;
  • Sedative medication causing hypercapnia (\> 3 drugs or more than 20mg of morphine/day);
  • Polygraphic diagnosis of Obstructive Sleep Apnoea Syndrome (AHI\>30/h (French criteria);
  • Cognitive impairment that would prevent informed consent into the trial
  • Pregnancy;
  • Tobacco use \< 10 pack-year;
  • Psychiatric disease necessitating anti-psychotic medication, ongoing treatment for drug or alcohol addiction, persons of no fixed abode post-discharge;
  • Unstable coronary artery syndrome;
  • Age \<18 years;
  • Inability to comply with the protocol;
  • Expected survival\<12 months due to any situation other than COPD disease;
  • Duration of ICU stay\>10 days;
  • No affiliated to national health insurance;
  • Measure of legal protection (guardianship, wardship or judicial protection) for patients over the age of majority.

Interventions

DEVICEhome ventilators

The 3 test treatments are home non-targeted NIV, home targeted NIV and rescue home NIV. COPD patients will be equipped with home ventilators and fitted with either nasal, oronasal or facial masks. All the ventilators used will be CE marked.


Locations(1)

Groupe Hospitalier Pitié Salpêtrière-Charles Foix

Paris, Île-de-France Region, France

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NCT03890224


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