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NCT07198880Not yet recruiting

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

Source: ClinicalTrials.gov · Last updated 30 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
40 (estimated)
First submitted
14 Sept 2025
Start date
1 Jan 2026
Primary completion date
1 Jan 2027
Lead sponsor
Assiut University
Diseases
COPD
NCT number
NCT07198880

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 1 Jan 2026 to the primary completion date, 1 Jan 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Undergone intubation or tracheostomy prior to NIV initiation during the last 2 months.
  • Those using addictive narcotic medications.

Other illness

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

Other

  • 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).

Who the study is looking for

  • 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

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.