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Recruiting NCT07467187

Invasive Home Ventilation in Denmark

— Observational Neuromuscular Diseases (NMD) ALS (Amyotrophic Lateral Sclerosis) Spinal Cord Injuries (SCI) Duchenne Muscular Dystrophy (DMD)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Neuromuscular Diseases (NMD), ALS (Amyotrophic Lateral Sclerosis), Spinal Cord Injuries (SCI), Duchenne Muscular Dystrophy (DMD). Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Evolution of Invasive Home Mechanical Ventilation in Denmark

Overview

The aim of this study is to describe national trends over the past 10 years in patients receiving invasive home mechanical ventilation (HMV) in Denmark. This includes indications for invasive HMV, diagnostic groups, and one-year mortality.

Primary outcome measures

  • Incidence of patients with invasive home mechanical ventilation [Time frame: Each year during the periode from 01.01.2016 to 12.31.2025]
Secondary outcome measures (3)
  • Prevalence of patients on home mechanical ventilation pr. year [Time frame: Each year during the periode from 01.01.2016 to 12.31.2025]
  • Number of new patients on invasive home mechanical ventilation per year [Time frame: Each year during the periode from 01.01.2016 to 12.31.2025]
  • One-year mortality [Time frame: Periode from 01.01.2016 to 12.31.2025]

Eligibility criteria

Inclusion criteria

  • Patients are included if they have or have had a respiratory certified personale care assistent during the period 2016-2025.

Exclusion criteria

  • Not tracheostomized
  • Tracheostomized but on spontaneous breathing throughout 1 January 2016 - 31 December 2025
  • Not discharged to home, assisted living, nursing home, or rehabilitation during 1 January 2016 - 31 December 2025

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Denmark · 1 center
  • Respiratory Center East — Copenhagen

Identifiers

NCT: NCT07467187 · p-2025-20512

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗