Impact of Home Non Invasive Ventilation in Patients With Chronic Obstructive Pulmonary Disease Di⦠(NCT07198880) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Impact of Home Non Invasive Ventilation in Patients With Chronic Obstructive Pulmonary Disease Discharged From Assiut University Hospital
40 participantsStarted 2026-01-01
Plain-language summary
This study aims to evaluate the impact of long-term home non-invasive ventilation (NIV) on patients with COPD
Who can participate
Age range18 Years ā 80 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients more than 18 year old.
* Severe COPD (classified as GOLD stage ā ¢ and IV), confirmed by FEVā/FVC \< 70% and FEVā \< 50% of the predicted value. (9)
* Persistent hypercapnia (PaCOā ā„ 60 mmHg ā„2 weeks after resolution of acute exacerbation and compliant on optimal medical therapy with or without long term oxygen therapy
Exclusion Criteria:
* 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).
* Pregnancy
* Refusal or Inability to tolerate NIV during initiation and adaptation phase.
* Expected Poor compliance (patients deemed unlikely to adhere to nightly NIV use such as no family support, severe frailty).
* Withdrawal criteria: stopping bipap or medical treatment, voluntary withdrawal by the participant, failure to attend scheduled visits, and significant clinical deterioration requiring alternative management during the study period