Impact of Home Non Invasive Ventilation in Patients With Chronic Obstructive Pulmonary Disease Discharged From Assiut University Hospital

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorAssiut University

About this trial

This study aims to evaluate the impact of long-term home non-invasive ventilation (NIV) on patients with COPD

Eligibility criteria

Qualifiers

Patients more than 18 year old.

Severe COPD (classified as GOLD stage Ⅲ and IV), confirmed by FEV₁/FVC < 70% and FEV₁ < 50% of the predicted value. (9)

Persistent hypercapnia (PaCO₂ ≥ 60 mmHg ≥2 weeks after resolution of acute exacerbation and compliant on optimal medical therapy with or without long term oxygen therapy

Disqualifiers

Other significant respiratory disorders (e.g,history suggestive OSA, Body Mass Index more than 30, pneumothorax, bullous lung disease, advanced interstitial lung diseases , restrictive thoracic wall diseases , neuromuscular disease).

Undergone intubation or tracheostomy prior to NIV initiation during the last 2 months.

Those using addictive narcotic medications.

Comorbidities and diseases that might confound survival outcomes (e.g., malignancy, advanced hepatic or renal diseases).

Trial design

Treatments tested in this trial

  • BiPAP device (non invasive ventilation)
  • Optimal Medical Management ( long acting beta agonist , long acting muscarinic antagonist and inhaled corticosteroids)

Treatment groups

40 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators