Skip to content

Initiation of home mechanical ventilation at home in a selectve group of patients with chronic hypercapnic respiratory failure in the Netherlands.

Initiation of home mechanical ventilation at home in a selectve group of patients with chronic hypercapnic respiratory failure in the Netherlands.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26822
Enrollment
96
Registered
2014-07-09
Start date
2014-12-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic ventilatory support

Interventions

The proposed intervention to be studied is initiation of HMV at home as compared to in hospital initiation I different settings. Recently a pilot study was performed in Groningen in which the initiati

Sponsors

Universital Medical Center Groningen Maastricht Universital Medical Center Universital Medical Center Utrecht Erasmus Medical Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Indication to initiate non-invasive ventilatory support in patients with a neuromuscular disease or thoracic cage abnormality who suffer from complaints of alveolar hypoventilation (fatigue, headache of dyspnoea) combined with all following elements: - arterial carbon dioxide > 6.0 kPa daytime or arterial or transcutaneous carbon dioxide > 6.0 kPa at night or orthopnea as a result of diaphragm paralysis - Age > 18 years - Existence, of a sufficient network (social or professional) according to the supervising HMV center making initiation of HMV at home possible and safe.

Exclusion criteria

Exclusion criteria: - Patients who already have had HMV due to acute respiratory failure - Necessity for invasive ventilatory support - Patients admitted to a nursing home

Design outcomes

Primary

MeasureTime frame
Primary objective: - Daytime arterial carbon dioxide (PaCO2) assessed without oxygen supplementation and ventilatory support while the patient is in sitting position

Secondary

MeasureTime frame
Secondary objective: - Health related quality of life - Lung function - Nocturnal transcutaneous carbon dioxide and saturation - Costs

Contacts

Public ContactAnda Hazenberg

Universitair Medisch Centrum Groningen Centrum voor Thuisbeademing

a.hazenberg@int.umcg.nl+31 (0)50 3614974 / +31 (0)50 3613200

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)